CN109803534A

CN109803534A - For treating the composition and method of inflammatory bowel disease (IBD) and other diseases

Info

Publication number: CN109803534A
Application number: CN201780043664.8A
Authority: CN
Inventors: T·J·鲍罗迪
Original assignee: Kleiston Holding Co
Current assignee: Kleiston Holding Co; Finch Research and Development LLC
Priority date: 2016-06-01
Filing date: 2017-06-01
Publication date: 2019-05-24
Also published as: US20210106629A1; JP2019520340A; EP3462882A1; US20170348360A1; AU2017274416B2; AU2017274416A1; CA3026414A1; EP3462882A4; WO2017210428A1; AU2017274416C1

Abstract

Present disclosure belongs to the field of medicinal compositions for being suitable for treating mammalian diseases.This application provides the new compositions and method for treating various illnesss relevant to the intestinal microbiota of functional disturbance or illness.Particularly, this application provides the compositions and method that can treat or cure stomach and intestine (GI) illness such as inflammatory bowel disease (IBD), including such as Crohn disease and ulcerative colitis.

Description

For treating the composition and method of inflammatory bowel disease (IBD) and other diseases

Cross reference to related applications

This application claims the U.S. Provisional Application No.62/344 that on June 1st, 2016 submits, 053 equity, the interim Shens It please be incorporated herein by reference in their entirety.

Technical field

This application provides for treating the new of various illnesss relevant to the intestinal microbiota of functional disturbance or illness Type composition and method.Particularly, this application provides can treat or cure stomach and intestine (GI) illness such as inflammatory bowel disease (IBD) The composition and method of (including such as Crohn disease and ulcerative colitis).

Background technique

Mammal contains multiple-microorganism species in its gastrointestinal tract (GI).Between these microorganisms and microorganism with Interaction between host, such as host immune system, mould microorganism.The micropopulation of health provides a variety of benefits for host Place, including colonizing resistance to broad spectrum of pathogens, it is necessary to nutrient biosynthesis and absorption, and maintain healthy gut epithelium With the immunostimulation of the general immunity of suitable control.Unbalanced micropopulation is (also referred to as " ecological disturbance " or that destroys be total to It is raw) it may lost its function and cause to increase the neurological susceptibility of pathogen, metabolic characteristics changes or induction can lead to part or complete The pro-inflammatory signals of body inflammation or autoimmunity.In addition, pathogen or disease that this micropopulation being destroyed may be entered Pathogen infection, this may cause the symptoms such as pain, diarrhea, gas and constipation.Therefore, intestinal microbiota is in such as enteropathic It plays an important role in the pathogenesis of many illnesss of sexuality dye.

People's faecal flora mass-planting is entered or is administered to be known as fecal microorganism transplanting (FMT) in the intestines of illness, generally also Referred to as fecal bacteria therapy.FMT is considered controlling key by creating a kind of ecological environment for being unfavorable for its proliferation and survival The various microorganisms of pathogen refill enteron aisle.It represents a kind of therapeutic scheme, can quickly rebuild normal composition and function It can property intestinal microflora.

Inflammatory bowel disease (IBD) is related to all or part of chronic infection in people digest road and inflammation.IBD mainly includes Ulcerative colitis and Crohn disease.Collagenous colitis, ischemic colitis, metastatic colitis, uncertain colitis, Microscopic colitis, mucous membrane colitis, pseudomembranous colitis and lymphatic colitis are usually also considered as inflammatory bowel disease.

Ulcerative colitis is the chronic disease of large intestine, also referred to as colon, wherein the inflammation of colon internal layer and is generated small Open ulcer or ulcer, generate fester and mucus.The combination of inflammation and ulcer can cause abdominal discomfort and frequently emptying Colon.The existing treatment of ulcerative colitis is related to strong and interminable composition of medicine treatment, with significant side effect or very It performs the operation to needs to remove segmental colonic.Therefore, it is necessary to more effective treatment of ulcerative colitis method, this method is easier It is administered and this situation for making one weakness can be cured.

Summary of the invention

In one aspect, this application provides pharmaceutical composition, it includes be able to suppress or antagonism Fusobacterium strain The non-pathogenic microorganism of a variety of work.On the other hand, pharmaceutical composition includes the non-pathogenic pula clostridium of one or more work spp.In one aspect, pharmaceutical composition includes fecal microorganism preparation, has and is supplemented with the non-pathogenic of one or more work The complete or essentially completed micropopulation of the donor of property pula clostridium spp.On the other hand, pharmaceutical composition also includes sterile Excrement filtrate.In one aspect, sterile faeces filtrate is originated from donor excrement.On the other hand, sterile faeces filtrate is from the micro- of culture Biology.

On the other hand, this application provides pharmaceutical composition, it includes be able to suppress or antagonism Fusobacterium species It non-pathogenic microorganism living and is able to suppress or more than second micro- lifes of non-cause of disease living of antagonism Mycobacterium species more than one Object.In one aspect, non-pathogenic microorganism living more than second include selected from anti-myco group it is one or more, two or more Kind, three or more, four kinds or more, five kinds or more, six kinds or more or seven kinds or more, by stick Shape bacillus, Dietzia, Gordonia, Mycobacterium, Nocardia, beam village Salmonella, Skermania, butyric acid tomb village bacterium, Turicella, Rhodococcus sp and Williamsia composition.On the other hand, pharmaceutical composition include with donor complete or The fecal microorganism preparation of essentially completed micropopulation.

In one aspect, the application provides pharmaceutical composition or kit, and it includes the excrement from single donor subject Just microorganism, application have one or more pula clostridium species or for the one or more of at least one pula clostridium species Growth stimulant, wherein the fecal microorganism relative to from do not apply the identical donors of one or more growth stimulants by The control fecal microorganism of examination person includes raised levels of at least one pula clostridium species.

On the other hand, this application provides the pharmaceutical compositions comprising non-synthetic fecal microorganism, wherein described non- It includes that raised levels of at least one is general that fecal microorganism, which is synthesized, relative to the control fecal microorganism from normal healthy donors Draw clostridium species.

In one aspect, this application provides the pharmaceutical compositions comprising non-selected fecal microorganism, wherein it is described not The fecal microorganism of the selection fecal microorganism non-selected relative to the control from normal healthy donors includes raised levels of At least one pula clostridium species.

On the other hand, this application provides pharmaceutical compositions, and it includes from the untreated of single donor subject Non-synthetic fecal microorganism, wherein untreated non-synthetic fecal microorganism is relative to the control excrement from normal healthy donors Microorganism includes raised levels of at least one pula clostridium species.

In one aspect, this application provides the method for the gastrointestinal disorder for the treatment of subject with this need, this method packets Include the pharmaceutical composition as described herein that pharmaceutical active dosage is applied to subject.In one aspect, the gastrointestinal disorder treated It is inflammatory bowel disease (IBD) or irritable bowel syndrome (IBS).

It in another aspect, should this application provides the method for the illness or illness for the treatment of subject with this need Method includes applying the pharmaceutical composition as described herein of pharmaceutical active dosage to subject and effectively treating the illness or shape Condition, wherein the obstacle or situation are selected from: acne, AIDS enteropathy, the relevant gastroenteritis of AIDS, whole body alopecia, old age are silly Slow-witted disease, amyloidosis, amyotrophic lateral sclerosis, ankylosing spondylitis, apositia, antibiotic-associated colitis, Asbergers syndrome, attention deficit disorder (ADD), attention deficit hyperactivity disorder (ADHD), autism spectrum disorder (ASD), Behcet syndrome, chronic clostridium difficile infection (CDI), chronic constipation, chronic depression, chronic fatigue syndrome (CFS), the false obstructive syndrome of chronic idiopathic, chronic inflammation Demyelinating Polyneuropathy, chronic nausea, chronic nettle Morbilli, celiaca, collagenous colitis, polyp of colon, constipation dominate FBD, Crohn disease, cryptogenic cirrhosis, circulation and vomit Spit, herpetic dermatitis, diabetes, familial Mediterranean fever, fatty liver, functional bowel disorder (FBD), gastroesophageal reflux, Gillian-Barre syndrome, glomerulonephritis, hemolytic uremic syndrome, halitosis, based on IBS constipation, IBS diarrhea/constipation Alternately, IBS based on diarrhea, IBS based on pain, Idiopathic Thrombocytopenic Purpura (ITP), idiopathic/simple constipation, Uncertain colitis, inflammatory bowel disease (IBD), irritable bowel syndrome (IBS), adolescent diabetes, Lyme disease, manicdepressive Disease, metabolic syndrome, microscopic colitis, migraine, Combination cryoglobulinemia, mucous colitis, multiple sclerosis, Myasthenia gravis, NASH (nonalcoholic fatty liver disease), non-rheumatoid arthritis, non-rheumatoid factor positive arthritis, Non-ulcer dyspepsia, Norwalk virus gastroenteritis, obesity, obsessive-compulsive disorder, pain, FBD, Parkinson's disease, more arteries Inflammation, polyposis, primary biliary cirrhosis, primary clostridial infection (CDI), primary sclerotic cholangitis (PSC), pseudomembranous colitis, psychiatric diseases, Reiter syndrome, recurrent diverticulitis, Rett syndrome, rheumatoid Arthritis, brandy nose, rotavirus gastroenteritis, sacro-iliitis, schizophrenia, chorionitis, Sjogren syndrome, intestinal bacteria Undue growth, unexpected infant death syndrome (SIDS), systemic loupus erythematosus we, ulcerative colitis, upper abdomen FBD, Vascular inflammatory disease, viral gastroenteritis, prediabetes syndrome, type-1 diabetes mellitus, type-2 diabetes mellitus, depression, spirit Split disease and emotional handicap.

In one aspect, this application provides in subject with this need treat IBD method, this method include to Subject applies the first antibiotic or the probiotics of pharmaceutical active dosage to inhibit or antagonism Fusobacterium species.

On the other hand, this application provides the method treated in subject with this need or cure IBD, this method packets It includes: removing the appendix of subject, apply biofilm disruption agent to subject, it is living to subject's administration of antibiotics, and application drug The pharmaceutical composition of the present invention of property dosage.

In one aspect, this application provides a kind of methods, comprising: the growth thorn of pula clostridium species is applied to subject Swash agent；Fecal specimens are collected from subject to prepare fecal microorganism composition.

Brief description

Fig. 1: phylogenetic tree, other exemplary F.prausnitzii of the display based on 16S rRNA gene order The relationship of other members of bacterium isolate and fusobacterium cluster IV (Ruminococcaceae).Sequence accession number is shown in bracket. It (adapts from Lopez-Siles et al., Appl.Environ.Microbiol.78:420-28 (2012)).

Detailed description of the invention

Unless otherwise defined herein, otherwise term should be understood according to the common usage of person of ordinary skill in the relevant.

All publications referred in this specification, patents and patent applications are both incorporated herein by reference, and degree is such as It is pointed out specifically and individually to be incorporated by reference into each individually publication, patent or patent application.

As herein and as used in the appended claims, singular " one ", "one" and "the" include plural number instruction Object, unless the context is clearly stated.As used herein, for embodiment, term " substantially ", phrase " substantially institute Have the peptide of array ", refer at least 90%, preferably at least 95%, more preferably at least 99%, and most preferably at least 99.9% Array peptide.Other purposes of term " substantially " are related to similar definition.

In the case where providing a series of values, it should be appreciated that each median between the upper and lower bound of the range with And described in any other in the range or median is included in the disclosure.These small range of upper and lower bounds It can be independently include in smaller range, and be also included in present disclosure, by any special row in the range The limitation removed.In the case where the range includes one or two limitation, the range other than the two limitations also includes In the disclosure.

As used herein, term " treatment " refers to (i) by preventing its development from completely or partially inhibiting embodiment Disease, illness or situation；(ii) by causing disease, illness and/or the recession of situation, alleviate embodiment completely or partially Disease, illness or situation；Or (iii) completely or partially prevent in patient may susceptible disease, illness and/or situation but still It is not diagnosed with disease, illness or situation.Similarly, " treatment " refers to therapeutic treatment and preventative or preventative arrange It applies.

As used herein, " therapeutically effective amount " or " pharmaceutical activity dosage " refer to effectively treat the disease, illness or The amount of the composition of situation.

As used herein, " micropopulation " and " flora " refers to sustainable and is briefly present in subject's body Or the microbiologic population on body, including eucaryote, archeobacteria, bacterium and virus (including bacterial virus (i.e. bacteriophage)). " fecal microorganism " or " fecal microorganism preparation " refers to the microbiologic population being present in subject's excrement.Non-selected excrement Microorganism refers to group or the mixture of the fecal microorganism from the fecal specimens derivative and processing of donor, does not select any spy The microorganism of fixed group or type, and it is substantially similar to the microbe composition found in this fecal specimens and group's knot Structure.

As used herein, " sterile excrement filtrate " or " acellular excrement filtrate " refers to the liquid component of fecal materials, wherein Liquid component free or substantially free of the biology (such as bacterium, fungi or its spore) based on cell, but retain bacteriophage and Acellular biomaterials.Preferably, acellular or sterile excrement filtrate are also free of virus for eukaryotic host cell.

As used herein, " growth stimulant " or " growth stimulant " is the life for referring to promote or enhance target organism The substance of long, proliferation or vigor.

As used herein, " alleviate, cure or fix-rate " refers to for given treatment and cures or alleviated or complete It totally disappeared the percentage for moving back the patient of illness.Alleviation, healing or the recession of ulcerative colitis refer to stops hemoproctia, urine completely Anxious and times of defecation increases.Quantitatively, when the UCDAI of patient scoring is less than or equal to 2, reach alleviation, healing or recession, It is assessed after treatment 8 weeks.It can further confirm to alleviate, cure or subside by endoscope and mucous membrane healing.

As used herein, " response rate ", which refers to, is positive (for example, one or more symptoms is tight to given treatment Weight degree or frequency reduce) patient's percentage.Quantitatively, when the UCDAI scoring of patient reduces at least 2 from baseline to the 8th week When, patient for treatment has positive reaction.

As used herein, " ulcerative colitis disease activity index " or " UCDAI " refer to for assessing exedens knot The symptom severity of enteritis patient or the index system of reaction.Four variables of the Index Assessment, including times of defecation, bleeding are tight The net assessment (table 1) of weight degree, mucous membrane of colon appearance and doctor to disease activity.Referring to Sutherland et al., 5- Aminosalicylic acid enema in the treatment of distal ulcerative colitis, proctosigmoiditis,and proctitis.Gastroenterology.1987；92:1894–8.Each variable It is divided into 0-3, therefore combined index score range is 0-12；0-2: alleviate；3-6: mild；7-10: mild；> 10: serious exedens Colitis.

As used herein, " eucaryote " refers to the cell belonged to comprising nucleus and film combination cell device.

As used herein, " bacterium ", " bacterial flora " and " archeobacteria ", which refers to, lacks film combination cell core and lacks cell The unicellular prokaryotic of device.

As used herein, " Colony Forming Unit " (cfu) refers to the estimation of viable microbial cells quantity in given sample. The quantity that cfu can be assessed by the clump count on Count Agar plate, as determining live bacterial cell number in sample Standard method.

As used herein, " feasible " means the ability for possessing procreation.It can be monitored according to the film integrality of cell The vigor of bacterial flora.Cell with impaired film is considered dead or dead, and the cell with complete film is considered It is living.For embodiment, SYTO 9 and propidium iodide are for dyeing and separating bacterium living and dead bacterium.Referring to Stocks, Cytometry A.2004Oct；61 (2): 189-95.Cell viability can also be assessed by molecular activity analysis, such as base In the method for PCR, nucleic acid relevant to living cells can be distinguished with nucleic acid relevant with killed cells.Referring to Cangelosi and Mescheke, Appl Environ Microbiol.2014 October；80 (19): 5884-5891.

As used herein, " separation " or " purifying " refers to bacterium or other entities or substance, (1) with most Just relative at least some components separation when production (either nature still in experimental situation), and/or (2) by Artificial manufacture, preparation, purifying and/or manufacture.The bacterium of isolated or purified can from least about 10%, about 20%, about 30%, about 40%, about 50%, about 60%, about 70%, about 80%, about 90% or more with its initially associated other components bacterium in point It separates out and.

As used herein, " cytotoxicity " activity or bacterium indicate to kill the ability of bacterial cell, such as pathogenic bacteria Cell." cell inhibition " activity or bacterium include inhibiting, partially or completely inhibiting bacterial cell (such as pathogenic bacteria cell) The ability of growth, metabolism and/or proliferation.

As used herein, about bacterium or any other organism or the term " pathogen " and " pathogenic " packet of entity Include any such organism of the disease that can cause or influence the host organism containing the organism or entity, illness or situation Or entity.

As used herein, " spore " or " spore " population includes bacterium (or other the unicellular lifes that can usually survive Object), than identical bacterium trophosome more resistant to affected by environment such as hot and fungicide, and usually can germinate and go out increase. The bacterium of " sporogenesis object " or " being capable of forming spore " is the bacterium containing gene and generates spore in suitable environmental conditions Other necessary abilities of son.

As used herein, " combination " of two or more bacteriums includes that the physics of two kinds of bacteriums coexists, identical In material or product or in the product of physical connection and the temporary co-administration or common location of two kinds of bacteriums.

1. stool frequency	Score distribution
		Normally	0
1-2 stool/day > normal	1
		3-4 stool/days > normal	2
> 4 stool/days > normal	3
		2. hemoproctia
Nothing	0
		Bloodstain	1
Apparent blood	2
		Mainly blood	3
3. mucous membrane appearance
		Normally	0
It is slight fragile	1
		Appropriateness is fragile	2
Exudation, hematostaxis	3
		4. evaluation of the doctor to disease activity
Normally	0
		Mildly	1
It is medium	2
		Seriously	3

1 ulcerative colitis of table (UC) disease activity index.See the Am J Gastroentero of Tursi et al., 105: 2218–27(2010)。

As used herein, " subject " refers to any animal subjects, including the mankind, experimental animal (such as primate Animal, rat, mouse), (such as dog, cat, grinding tooth are dynamic for livestock (such as ox, sheep, goat, pig, turkey, chicken) and house pet Object etc.).Subject or patient may be health, with infection or may may perhaps have due to gastrointestinal pathogen Development or the risk that the infection due to caused by gastrointestinal pathogen is propagated to other people.

As used herein, " Shannon diversity index " refers to using formulaCalculate object in specific group The abundance of kind and the diversity indices of the uniformity, wherein H is Shannon diversity indices, and R is the sum of species in group, pi It is by the ratio of the R of i-th kind of species composition.Higher value indicates community that is different and being evenly distributed, and being worth indicates for 0 given There is only a species in community.For with further reference to Shannon and Weaver, (1949) The mathematical Publishing house, the University of Illinois theory of communication., Urbana.117pp.

As used herein, " antibiotic " refers to for by killing bacterium, inhibiting bacterial growth or reducing bacterial action To treat and/or prevent the substance of bacterium infection.

As used herein, " intermittent dosing regimen " refers to therapeutic combination administration a period of time, when being then administered one section Between (treatment phase), wherein stop with this therapeutic combination treatment (rest period).Intermittent dosing regimen is represented by treatment phase, with It or week/rest period, by day or in terms of week.For embodiment, 4/1 intermittent dosing regimen refers to intermittent dosing regimen, wherein treating Phase is four weeks/day, and the rest period is one week/day.

As used herein, " continuous dosing regimens " refer to dosage regimen, and wherein therapeutic combination is administered during treatment Without the rest period.During the entire treatment of continuous dosing regimens, therapeutic combination can be given；For embodiment, daily, Or every other day, or every three days.In that day of application therapeutic combination, it can be applied in one day with single dose or multi-dose With.

As used herein, " administration frequency " refers to the frequency that therapeutic combination dosage is given within given time.Administration Frequency can be expressed as the dosage number of per given time；For embodiment, once a day, once a week or biweekly.

As used herein, " dosing interval " refers to the elapsed time amount between the multi-dose for giving subject.

Ulcerative colitis is a kind of disease characterized by large intestine shallow-layer inflammation and microulceration.Inflammation usually occurs Rectum and colon lower part, but it may influence entire large intestine (pancolitis).Ulcerative colitis has little effect on its distal portions Small intestine (backwash ileitis).

For inflammation along with diarrhea, diarrhea may be loose and bloody.It is formed in the place of inflammatory destruction intestinal cell small Ulcer；These region bleedings simultaneously generate fester and mucus.Ulcerative colitis, especially slight ulcerative colitis may It is difficult to diagnose, it is most notably another to be known as Crohn disease and intestines easily swash synthesis because symptom is similar with other intestines problems The IBD of sign.Crohn disease is different from ulcerative colitis, because it causes inflammation and generate deep to burst in entire intestinal wall thickness Ulcer.Crohn disease usually occurs in small intestine, but may also occur in large intestine, anus, esophagus, stomach, appendix and oral cavity.Crow grace Disease causes fistula, and ulcerative colitis then will not.Crohn disease and ulcerative colitis may coexist in same patient.

Ulcerative colitis occurs most often in 15 to 30 years old crowds, although this disease may torment any age People.It coequally affects men and women, and seems popular in certain families.

There are different types of ulcerative colitis.As used herein, " proctitis ulcerosa " refers to that intestinal inflammation limits to In the disease form of rectum.Due to its limited range (usually less than six inches of rectum), proctitis ulcerosa is often one The slighter ulcerative colitis of kind.It is related to less complication, and provides prospect more better than wider disease.It is right In about 30% patients of ulcerative colitis, which starts from proctitis ulcerosa.

As used herein, " proctosigmoiditis " refers to a kind of colitis for influencing rectum and sigmoid colon, colon Lower section is located above rectum.Symptom includes bloody diarrhea, spasm and persistently feels to need through excrement, referred to as tenesmus.Abdomen The moderate pain of portion lower left is likely to occur in active disease.

As used herein, " left sided colitis " refers to since rectum and extends to the curved company of the colon near spleen Continuous inflammation, referred to as spleen are bent.Symptom includes loss of appetite, weight loss, diarrhea, the severe pain of abdomen left side and bleeding.

As used herein, " general ulcer (total) colitis " influences entire colon.Symptom include diarrhea, serious abdominal pain, Spasm and extensive weight loss.Potential severe complication includes bleeding profusely and colon acute dilatation (the huge knot of Poisoning Intestines), it is open that this may cause intestinal wall.Serious complication may need to perform the operation.

Several theories have been proposed about the reason of ulcerative colitis.Evidence suggests the immune system meetings of body Reaction is generated to the environment, diet or infectious agent of inheritance susceptible individual, leads to intestinal wall inflammation.Ulcerative colitis is not by certain Caused by emotional disturbance caused by a little foods or food or sensibility, but these factors may cause the symptom of certain people.It bursts Ulcer colitis is most likely not abnormal response, but is infected.

The most common symptom of ulcerative colitis is bloody diarrhea and abdominal pain.Patient be also possible that fever, hemoproctia, Fatigue, anaemia, loss of appetite, weight loss and body fluid and nutrient loss lead to nutritional deficiency.These symptoms disappear in symptom Intermittent attack (breaking out) occurs during losing (alleviation).These are without even several years stadium sustainable several months.In general, breaking-out is opened The urgent of defecation increases when the beginning, slight lower abdomen spasm, blood and mucus in excrement.

Ulcerative colitis may cause long-standing problem, as (fatty liver, hepatitis, liver are hard for arthritis, inflammation of eye section, hepatopathy Change and primary sclerotic cholangitis), osteoporosis, fash, anaemia and kidney stone.When immune system causes other portions of body When the inflammation of position, it may occur that these complication.When effectively treatment colitis, these problems may disappear.

The treatment of ulcerative colitis depends on the severity of disease.Most people all receives drug therapy.Some diseases The people that shape is caused by certain foods can control symptom, such as the food of height seasoning by avoiding the food for making enteron aisle discomfort Or dairy products.Everyone can undergo different ulcerative colitis, therefore treat for everyone.

Many receives 5-ASA drug therapy with slight or moderate disease patient first, including 5- aminosalicylic acid and The combination of salicylazosulfapyridine class drug, helps to control inflammation.Salicylazosulfapyridine is most common in these drugs.Willow nitrogen Sulfapryidine can according to need use, can also be used together with other drugs.It is bad to salicylazosulfapyridine therapeutic effect Patient newer 5-ASA drug may be reacted.The possibility side effect of 5-ASA preparation includes Nausea and vomiting, stomach Scorching hot, diarrhea and headache.

People with serious disease and the corticosteroid treatment that the unresponsive people of 5-ASA preparation can be used addition. Prednisone, budesonide and hydrocortisone are the corticosteroids for mitigating inflammation.According to the position of inflammation, they can be with Oral, intravenous injection, bowel lavage or suppository administration.Corticosteroid can cause side effect, as weight gain, acne, facial hair, Hypertension, diabetes, mood swing and infection risk increase, therefore doctor can carefully monitor the patient for taking these drugs.

Usually using immunosuppressor such as imuran, Ismipur (6-MP) and methotrexate (MTX), and can be low Significant improvement, side effect are seldom under dosage.Other drugs can be given so that patient loosens or mitigate pain, diarrhea or infection. Once in a while, serious symptom is to being enough to make patient's hospitalization.For embodiment, a people may have severe haemorrhage or severe diarrhea to lead Cause dehydration.In this case, doctor can attempt to prevent the loss of diarrhea and blood, liquid and mineral salt.Patient may need Special diet is fed by vein, drug therapy or is sometimes performed the operation.

In severe cases, patient may need to perform the operation to remove the colon of illness.If therapeutic treatment failure or skin The side effect of matter steroids or other drugs threatens the health of patient, and doctor suggests removing colon sometimes.

It is previous observation indicate that certain Fusobacterium enteric infections (for example, by F.varium, F. nucleatum or Actinomyces pseudonecrophorus) and ulcerative colitis between potential association.See, for example, Ohkusa et al., Gut.52 (1): 79-83 (2003)；Sasaki and Klapproth, Journal of Signal Transduction, vol.2012, Article ID 704953,6pages,(2012)； Allen-Vercoe,Digestive Diseases and Sciences,60(1):7-8 (2015).Fusobacteria is anaerobic Gram-negative rods, no spore, and elongated cell has tapered distal end or multiform Property.Fusobacterium spp. is a part of the normal flora of oropharynx, gastrointestinal tract and genital tract.Operation or accident trauma, It may be infected after oedema, anoxic, disorganization and animal bite.Particularly, with Crohn disease (16%) or other compare (3-13%) is compared, and F.varium is considered in the mucous membrane of colon for being present in the high proportion (84%) of patients of ulcerative colitis. Referring to Ohkusa et al. J Gastroenterol Hepatol 17:849-53 (2002).Ohkusa et al. (2003) is also asserted The F.varium induced mouse model Experimental oral ulcer colitis separated from colonic mucosa from patients with ulcerative. Gut.52(1):79–83(2003)。

Meanwhile F.nucleatum be recognized as it is related with ecphyaditis.Referring to Allen-Vercoe et al., Gut Microbes.2:294–98(2011).For embodiment, F. nucleatum and downright bad shuttle bar are observed in acute appendicitis The part invasion of bacterium.Referring to Swidsinski et al., Gut, 60:34-40 (2011).Particularly, Swidsinski et al. is used Fluorescence in situ hybridization based on rRNA has studied the slice that ecphyaditis is made a definite diagnosis in 70 attachmentes, and discovery bacterium deeply infiltrates appendix. In 62% patient, Fusobacterium (mainly F.nucleatum and actinomyces pseudonecrophorus) is the specific of epithelium and submucosal infiltration Ingredient, and do not found in various controls.The presence of Fusobacterium and the severity of ecphyaditis are positively correlated.On the contrary, main Fecal microorganism include bacteroid, rectum fungi (clostridium group XIVa), pula clostridium group and Ackermam bacterium The significant decline of muciniphila, inversely with the severity of ecphyaditis.

Studies have reported that being associated between analysis appendectomy and ulcerative colitis, and it is most of research shows that depositing In very significant inverse relation.Referring to Roblin et al., Gut, 61:635-36 (2012).In particular, it is said that appendectomy Art treats diseases associated with inflammation (ecphyaditis or lymphnoditis) rather than the non specific abdominal pain then risk with subsequent ulcerative colitis It is lower related.In addition, the inverse relation is limited to the patient to undergo surgery before 20 years old.Referring to Andersson et al., N Engl J Med；344:808-14 (2001).Therefore, the development of appendix ecological disturbance may be the initiation thing that ulcerative colitis occurs Part.Removal appendix can reduce the risk that ulcerative colitis further develops in inheritance susceptible individual.

Although the above-mentioned correlation (for example, ulcerative colitis) about between Fusobacterium enteric infection and IBD Assert, but for the best knowledge of applicant, until the application does not also test or prove to inhibit Fusobacterium enteron aisle Infection can treat IBD.

In one aspect, present disclose provides the drugs for treating IBD or other illnesss in subject in need Composition and its method or purposes, wherein the composition include it is a variety of be able to suppress or the work of antagonism Fusobacterium strain it is non- Pathogenic microorganism.In one aspect, pharmaceutical composition includes the non-pathogenic microorganism of a variety of work, to one or more Fusobacteriums Belong to strain and shows cytotoxicity or cell inhibitory activity.In one aspect, pharmaceutical composition includes from synthesis culture The non-pathogenic microorganism of a variety of work.In one aspect, repressed Fusobacterium strain is selected from actinomyces pseudonecrophorus, tool core shuttle bar Bacterium, F.canifelinum, F.gonidiaformans, fusobacterium mortiferum, F.naviforme, fusobacterium necrogenes, F.russii, Ulcer Fusobacterium and F.varium.On the other hand, repressed Fusobacterium strain is selected from F.nucleatum, actinomyces pseudonecrophorus And F.varium.

Pula clostridium is one of the most abundant bacterium in human intestine's ecosystem, and quantitative range is healthy individuals excrement In total micropopulation 5-20%.Key supplier of the F.prausnitzii bacterium butyrate to colonic epithelium. F.prausnitzii bacterium is initially classified as Fusobacterium prausnitzii.However, different mankind's bacterial strain (ATCC 27766 and ATCC 27768) the complete sequence of 16s rRNA gene confirm them only edge remote to Fusobacterium be related simultaneously And it is more closely related with the member of clostridium cluster IV (clostridium leptum race).2002, Duncan et al. proposed a kind of new general Draw clostridium Pseudomonas, including non-sporogenesis and non-athletic gram-positive bacterium, entitled pula clostridium.Referring to Duncan etc. People, Int J Sys Evol Microbiol 52:2141-46 (2002).According to 16S rRNA Phylogenetic Analysis, pula shuttle Bacterium Pseudomonas is the member of Ruminococcaceae family, is named as Clostridiales, the clostridium in Firmicutes Belong to (Clostridia).F. prausnitzii bacterium is considered as stringent anaerobic bacteria, two minutes after being exposed to surrounding air Inside lose vigor.Referring to Duncan et al., Int J Sys Evol Microbiol 52:2141-46 (2002).Illustratively Pula clostridium species and bacterial strain are listed in table 2 and Fig. 1.

Table 2: exemplary pula clostridium bacterium

F.prausnitzii bacterium is announced shows anti-inflammatory effect using mouse colitis model in vitro and in vivo.It is special Not, it is desirable that application F.prausnitzii strains A 2-165 and its culture supernatants are to prevent 2 in mouse, 4,6- tri- nitre The colitis of base benzene sulfonic acid (TNBS) induction.Referring to Sokol et al., Proc Natl Acad Sci USA105:16731-36 (2008).In addition, Varela et al. assert maintenance that F. prausnitzii bacterium level and ulcerative colitis (UC) are alleviated it Between exist association.Observe F.prausnitzii bacterium number amount lower than normal healthy controls in the UC patient of alleviation.Meanwhile still locating F.prausnitzii bacterium number amount in the UC patient of paracmasis is higher than patients with recurrent.Referring to Varela et al., Alimentary pharmacology&therapeutics, 38:151-61 (2013).In addition to F.prausnitzii bacterium, Machiels et al. also reported another species caecum Ross Salmonella hominis patients of ulcerative colitis for producing butyrate It reduces, and claims that caecum Ross Salmonella hominis may also play a role in UC.See Machiels et al. Gut, 63:1275- 83(2014)。

Equally, in spite of above-mentioned observation or report about F.prausnitzii bacterium, but with regard to the best knowledge of applicant and Speech, it be not both proposed or without passing through test, needless to say demonstrated, until F.prausnitzii living in the application Bacterium can be used for treating IBD.Not by any scientific theory, F.prausnitzii bacterium living inhibit or antagonism enteric infection in The growth of Fusobacterium.

In one aspect, present disclose provides the drugs of IBD or other illnesss for treating subject with this need Composition and its method or purposes, wherein the composition includes the non-of a variety of work comprising one or more pula clostridium species Pathogenic microorganism.In one aspect, pharmaceutical composition includes the non-pathogenic pula clostridium of a variety of work.In one aspect, drug Composition include a variety of work non-pathogenic microorganism, it includes it is one or more, two or more, it is three or more, four Kind or more, five kinds or more, six kinds or more or seven kinds or more strains selected from the group below, isolate or Strain: pula clostridium prausnitzii A2-165, pula clostridium prausnitzii ATCC 27768, pula clostridium Prausnitzii ATCC 27766, pula clostridium cf.prausnitzii KLE1255, pula clostridium prausnitzii L2- 6, pula clostridium prausnitzii M21/2, pula clostridium prausnitzii SL3/3, pula clostridium sp.canine oral Taxon 147, pula clostridium sp. DJF_VR20, pula clostridium sp.MC_41, pula clostridium sp.CAG:1138, pula clostridium Sp. CAG:74 and pula clostridium sp.CAG:82.In one aspect, pharmaceutical composition includes the non-pathogenic microorganism of a variety of work, It includes it is one or more, two or more, three or more, four kinds or more, five kinds or more, six kinds or more The bacterial strain listed in a variety of or seven kinds or more pula clostridium species, isolate or Fig. 1.

On the other hand, pharmaceutical composition also includes the growth stimulant of pula clostridium bacterium.In one aspect, pharmaceutical composition Growth stimulant comprising being selected from apple pectin, N-acetyl-glucosamine, cysteine, glutathione, riboflavin and flavine.Mostly Count the F.prausnitzii bacterial strain well-grown on apple pectin under anaerobic.See Lopez-Siles et al., Appl.Environ.Microbiol.78:420-28 (2012).Pectin ferments extensively in people's colon.It is some F.prausnitzii bacterial strain is grown using uronic acid.Therefore, the application using rich pectous substrate or uronic acid come into The enhancing of one step is for stimulating the prebiotics method of F.prausnitzii bacterium growth and therapeutic effect.

Purposes present invention also provides excrement donor as bioreactor, for generating the full spectrum microorganism of modification Group is for use as more effective therapeutic agent.In one aspect, invention further provides a kind of methods, including apply to subject The growth stimulant of pula clostridium species；Fecal specimens are collected from the subject to prepare fecal microorganism composition, wherein The fecal microorganism composition includes (not take institute relative to control fecal microorganism group's composition from same subject State growth stimulant) the raised levels of pula clostridium species.In one aspect, thorn is grown described in subject's orally ingestible Swash agent.In one aspect, growth stimulant is selected from apple pectin, N-acetyl-glucosamine, cysteine, glutathione, riboflavin And flavine.Referring to US2015/0283144.In one aspect, at least about 1 after applying the growth stimulant, 2,3,4,5,6, 7,8,9,10,11,12,13,14,18,20,24,28,30,36 hours collection fecal specimens.On the other hand, described in the application At least about 1 after growth stimulant, 2,3,4,5 or 6 days collection fecal specimens.In one aspect, collect the fecal specimens it Before, growth stimulant was applied to the subject more than about 1,2,3,4,5,6,7,8,9,10,11,12,13 or 14 day.Another On one side, before collecting the fecal specimens, by growth stimulant be applied to the subject be more than 1,2,3,4,5,6, 7,8,9,10,11,12,13 or 14 weeks.In one aspect, growth stimulant at least 1,2,3,4,5,6,7,8,9 or 10 time daily It is applied to the subject.In one aspect, by the method prepare fecal microorganism composition with come from it is identical tested The control fecal microorganism (not applying growth stimulant) of person compares, and includes 1.5 times or more, 2 times or more, 2.5 Times or more, 3 times or more, 3.5 times or more, 4 times or more, 5 times or more, 10 times or more, 50 Times or more, 100 times or more, 1000 times or more, 10,000 times or more of pula clostridium bacterium.In another party Face (does not have by fecal microorganism composition prepared by the method relative to the control fecal microorganism from same subject Have the application growth stimulant), comprising at least 10% or more, 15% or more, 20% or more, 25% or more, 30% or more, 40% or more, 50% or more, 60% or more, 70% or more, 80% or more, 90% or more, 100% or more, 150% or more, 200% or more, 250% or more, 300% or more, 350% or more, 400% or more, 450% or more, 500% or more, 600% Above, 700% or more or 800% or more pula clostridium bacterium.On the other hand, the present invention also provides a kind of method, packets It includes: applying one or more pula clostridium species to subject；Fecal specimens are collected from the subject to prepare the micro- life of excrement Compositions, wherein the fecal microorganism composition includes relative to the control fecal microorganism combination from same subject One or more raised levels of pula clostridium species of object (not taking one or more pula clostridium species).

In one aspect, present disclose provides pharmaceutical compositions, and it includes the micro- lifes of excrement from single donor subject Object, the fecal microorganism application has one or more growth stimulants of at least one pula clostridium species, wherein the excrement Just microbial is micro- for the control excrement from the identical donor subject for not applying one or more growth stimulants Biology includes the raised levels of pula clostridium species of at least one.In one aspect, donor subject absorbs a kind of or more Kind growth stimulant.On the other hand, one or more growth stimulants be selected from apple pectin, N-acetyl-glucosamine, cysteine, Glutathione, riboflavin and flavine.In one aspect, fecal microorganism come from least about 1 after applying the growth stimulant, 2,3,4,5,6,7,8,9,10,11,12,13,14,18,20,24,28,30 or 36 hours fecal specimens collected.In another party Face, fecal microorganism is from least about 1,2,3,4,5 or 6 day excrement sample collected after the application growth stimulant Product.In one aspect, by one or more growth stimulants be applied to the donor subject more than about 1,2,3,4,5,6,7, 8,9,10,11,12,13 or 14 days.In one aspect, one or more growth stimulants the donor subject is applied to surpass Spend about 1,2,3,4,5,6,7,8,9,10,11,12,13 or 14 week.In one aspect, daily at least 1,2,3,4,5,6,7,8, Give the one or more growth stimulants of the donor subject 9 or 10 times.On the other hand, in need the present invention provides treating Patient IBD (such as UC) treatment method, wherein this method includes giving patient's one or more pula clostridium bacterium growth Stimulant, one or more bile acid sequestrants (for example, cholestyramine, colestipol, colesevelam), or both, into one Step applies pharmaceutical composition as described herein (for example, the non-selected fecal microorganism from single donor subject, application There are one or more pula clostridium bacterium growth stimulants).

In one aspect, present disclose provides the pharmaceutical compositions comprising non-synthetic fecal microorganism, wherein the non-conjunction Include raised levels of at least one pula relative to the control fecal microorganism from normal healthy donors at fecal microorganism Clostridium species.On the other hand, present disclose provides the pharmaceutical compositions comprising non-selected fecal microorganism, wherein relative to The non-selected fecal microorganism of control from normal healthy donors, the non-selected fecal microorganism include raised levels of At least one pula clostridium species.On the other hand, this disclosure provides pharmaceutical compositions, and it includes supply from single The untreated non-synthetic fecal microorganism of body subject, wherein the untreated non-synthetic fecal microorganism is relative to coming from The control fecal microorganism of normal healthy donors includes raised levels of at least one pula clostridium species.

In an aspect, the elevated levels are selected from 1.5 times or more, 2 times or more, 2.5 times or more Again, 3 times or more, 3.5 times or more, 4 times or more, 5 times or more, 10 times or more, 50 times or more, 100 Times or more, 1000 times or more and 10,000 times or more.In another aspect, the elevated levels are selected from least 10% or more, at least 15% or more, at least 20% or more, at least 25% or more, at least 30% or more, at least 40% or more, extremely Few 50% or more, at least 60% or more, at least 70% or more, at least 80% or more, at least 90% or more, at least 100% or more, At least 150% or more, at least 200% or more, at least 250% or more, at least 300% or more, at least 350% or more, at least 400% or more, at least 450% or more, at least 500% or more, at least 600% or more, at least 700% or more, and is at least 800% or more.

Mycobacterium avium, subspecies paratuberculosis (MAP) cause milk cow and various other animals Enteron aisle chronic disease, including non-human primate, referred to as Johne (" YO- knee ") disease.Pass through cd patient Various technologies determine always MAP.The existing research of MAP in cd patient is investigated often in " feminine gender " ulcerative colitis MAP is found in control, shows that ulcerative colitis is also as caused by MAP.For embodiment, a research report is said, when from When the different parts of enteron aisle obtain multiple samples, in Crohn disease and patients of ulcerative colitis, Mycobacterium The illness rate of avium and subspecies paratuberculosis infection is respectively 82.1% and 40%.Referring to Pistone et al., Digestive and Liver Disease 44:461–65(2012).Other than this observation result, Pierre's Si also vacation before this If MAP may be the pathogen of ulcerative colitis and Crohn disease, it is intended to explain both diseases common epidemiology, Reason distribution and familial and sporadic cluster.See Pierce, Gut Pathog.2:21 (2010).According to the saying of Pierre Si, When infecting MAP, a cognition infects the gene of clinical manifestation according to dosage, approach, age, gender and MAP and develops as ulcer Property colitis or Crohn disease.

Dietzia subspecies C79793-74 is formerly known as mycobacterium tuberculosis (Mycobacterium gordonae), according to It is reported under condition of in vitro culture and inhibits MAP.Referring to Richards (1989) in Johne ' s Disease:Current Trends in research, diagnosis and management, in the beast of Victoria,Australia Parkville The proceeding that doctor research institute holds, Milner and Wood are edited；Click and Van Kampen, J.Dairy Sci.92: 4846-51(2009)；United States Patent (USP) No.8,414,886.Dietzia belongs to one group of putting containing mycolic acid together with mycobacteria Line bacterium, including such as corynebacteria, Dietzia, Gordonia, mycobacteria, Nocard's bacillus, beam village Salmonella, Skermania, Butyric acid tomb village bacterium, Turicella, Rhodococcus sp and Williamsia (being referred to as " anti-myco bacterium " hereafter) etc. belong to.Referring to Bergey's Manual of Systematic Bacteriology, volume 5 (2012): Actinobacteria, the 246th, Page 291,302,313,378,436,438,470 and 501.

In conjunction with Fusobacterium explained above, ecphyaditis, appendectomy, ulcerative colitis, MAP, resist Connection between myco bacterium and Crohn disease, the application further provide following for treating and curing Crohn disease and burst The composition and method of ulcer colitis.

In one aspect, present disclose provides the drugs for treating IBD or other illnesss in subject in need Composition and its method or purposes, wherein the composition includes to be able to suppress or more than first of antagonism Fusobacterium species living Non-pathogenic microorganism and be able to suppress or more than second non-pathogenic microorganisms living of antagonism Mycobacterium.A side Face, more than first non-pathogenic microorganism living show cytotoxicity or the cell suppression for one or more Fusobacterium species System activity.In one aspect, first, second or two kind of a variety of work non-pathogenic microorganism from synthesis culture.A side Face, repressed Fusobacterium species be selected from actinomyces pseudonecrophorus, Fusobacterium nucleatum, F. canifelinum, F.gonidiaformans, fusobacterium mortiferum, F.naviforme, fusobacterium necrogenes, F.russii, ulcer Fusobacterium and F.varium.In another aspect, repressed Fusobacterium species be selected from F.nucleatum, actinomyces pseudonecrophorus and F.varium.In an aspect, repressed Mycobacterium species are Mycobacterium avium ssp.paratuberculosis(MAP).In an aspect, non-pathogenic microorganism living more than first, more than second it is living Non-pathogenic microorganism or both is in anaerobism packaging or container.In another aspect, non-pathogenic microorganism living more than first, More than second non-pathogenic microorganism living or both is in aerobic packaging or container.

In an aspect, more than first non-pathogenic microorganism living includes one or more pula clostridium species.One In a aspect, more than first non-pathogenic microorganism living includes pula clostridium.In an aspect, more than first non-cause of disease living Microorganism include it is selected from the group below it is one or more, two or more, it is three or more, four kinds or more, five kinds or More kinds of, six kinds or more or seven kinds or more strains, isolate or bacterial strain: pula clostridium prausnitzii A2- 165, pula clostridium prausnitzii ATCC 27768, pula clostridium prausnitzii ATCC 27766, pula clostridium It is cf.prausnitzii KLE1255, pula clostridium prausnitzii L2-6, pula clostridium prausnitzii M21/2, general Draw clostridium prausnitzii SL3/3, pula clostridium sp.canine oral taxon 147, pula clostridium sp.DJF_VR20, Pula clostridium sp.MC_41, pula clostridium sp.CAG:1138, pula clostridium sp.CAG:74 and pula clostridium sp.CAG:82.? In one aspect, more than first non-pathogenic microorganism living include listed in Fig. 1 it is one or more, two or more, three Kind or more, four kinds or more, five kinds or more, six kinds or more or seven kinds or more pula clostridium species, Isolate or bacterial strain.In another aspect, pharmaceutical composition also includes the growth stimulant of pula clostridium bacterium.In one aspect In, pharmaceutical composition includes to be selected from apple pectin, N- acetylglucosamine, cysteine, glutathione, riboflavin and Huang The growth stimulant of element.In an aspect, pharmaceutical composition is in anaerobism packaging or container.In another aspect, drug Composition also includes oxygen scavenger.

In an aspect, more than second non-pathogenic microorganism living is shown to one or more Mycobacterium species Cytotoxicity or cell inhibitory activity.In an aspect, cytotoxicity or cell inhibitory activity are directed to selected from the group below point Ramibacterium species: mycobacterium tuberculosis, M.leprae, M. avium-intracellulare, M.bovis, M.cheloiei、M.africanum、M.marinium、 M.buruli、M.fortuitum、M.haemophilum、 M.intracellulare、M.kansasii、 M.littorale、M.malmoense、M.marianum、M.sinuae、 M.szulgai and M. ulcerans, M.avium, M.flavascens, M.lepraemurium or M.nicroti.At one In aspect, cytotoxicity or cell inhibitory activity are for MAP.

In an aspect, non-pathogenic microorganism living more than second include it is selected from the group below it is one or more, two kinds or More kinds of, three or more, four kinds or more, five kinds or more, the bacterium of six kinds or more or seven kinds or more Kind: corynebacteria, Dietzia, Gordonia, mycobacteria, Nocard's bacillus, beam village Salmonella, Skermania, butyric acid tomb village bacterium, Turicella, Rhodococcus sp and Williamsia (being referred to as " anti-Myco " race).In another aspect, more than second non-disease living Pathogenic microorganism include it is selected from the group below it is one or more, two or more, three or more, four kinds or more of bacterium Kind: Dietzia, Gordonia, mycobacteria, Nocard's bacillus and Rhodococcus sp.' the bacterium of anti-Myco' group is aerobic.One In a aspect, these bacteriums and growth promoter such as trehalose, mannose, fructose or D-Glucose are co-administered, with preferably It survives in most of anaerobism intestinal environment.In another aspect, iron, copper and zinc component are added to enhance the life of these bacteriums It is long, coconut (Cocos nucifera L.) water that addition is moderately aged also can be used.Coconut water originates from after one and a half months Coconut fruit is the liquid that a kind of height is nourished, contain a large amount of chemical component: different sugar, sugar alcohol, inorganic ions, dimension are given birth to Element, lipid, amino acid, nitrogenous compound, organic acid, enzyme, plant hormone etc..Coconut water promotes the growth of anti-Myco bacterium.

In another aspect, non-pathogenic microorganism living more than second include it is one or more, two or more, three Kind or more, four kinds or more, five kinds or more, six kinds or more or seven kinds or more Dietzia strains, Bacterial strain or isolate.In another aspect, non-pathogenic microorganism living more than second include it is selected from the group below it is one or more, Two or more, three or more, four kinds or more, five kinds or more, six kinds or more or seven kinds or more Kind: D.aerolata, D.alimentaria, D.aurantiaca, D.cerdiciphylli, D.cinnamea, D.kunjamensis、D.lutea、D.maris、D.natronolimnaea、D.papillomatosis、 D.psychralcaliphila, D.schimae and D.timorensis.

In an aspect, non-pathogenic microorganism living more than second include it is selected from the group below it is one or more, two kinds or More kinds of, three or more, four kinds or more, five kinds or more, six kinds or more or seven kinds or more Gordonia strain: G.aichiensis, G.alkanivorans, G.amarae, G.amicalis, G.araii, G.bronchialis、G.defluvii、G.desulfuricans、 G.effusa、G.hirstuta、G.hydrophobica、 G.lacunae、G.malaquae、G. namibiensis、G.otitidis、G.paraffinivorans、 G.polyisoprenivorans、G. rhizosphera、G.rubripertincta、G.shandongensis、 G.sihwensis, G.sinesedis, G.soli, G.sputi, G.terrae and G.westfalica.

In an aspect, non-pathogenic microorganism living more than second include it is selected from the group below it is one or more, two kinds or More kinds of, three or more, four kinds or more, five kinds or more, the stick of six kinds or more or seven kinds or more Shape bacillus species: C.accolens, C.afermentans ssp. afermentans, C.ammoniagenes, C.amycolatum、C.appendicis、C.aquilae、 C.argentoratense、C.atypicum、 C.aurimucosum、C.auris、C.auriscanis、C.bovis、C.callunae、C.camporealensis、 C.canis、C.capitovis、C.casei、 C.caspium、C.ciconiae、C.confusum、C.coyleae、 C.cystitidis、C.diphtheria、 C.doosanense、C.durum、C.efficiens、C.falsenii、 C.felinum、C.flavescens、 C.freiburgense、C.freneyi、C.glaucum、 C.glucuronolyticum、C.glutamicum、 C.halotolerans、C.hansenii、C.imitans、 C.jeikeium、C.kroppenstedtii、C. kutscheri、C.lipophiloflavum、C.lubricantis、 C.macginleyi、C.marinum、 C.maris、C.massiliense、C.mastitidis、C.matruchotii、 C.minutissimum、 C.mucifaciens、C.mustelae、C.mycetoides、C.phocae、C.pilbarense、 C. pilosum、C.propinquum、C.pseudodiphtheriticum、C.pseudotuberculosis、 C.pyruviciproducens、C.renale、C.resistens、C.riegelii、C.simulans、C. singular、 C.sphenisci、C.spheniscorum、C.sputi、C.stationis、C.striatum、 C.suicordis、 C.sundsvallense、C.terpenotabidum、C.testudinoris、C. thomssenii、C.timonense、 C.tuberculostearicum、C.tuscaniense、C.ulcerans、 C.ulceribovis、C.urealyticum、 C.ureicelerivorans, C.variabile, C. vitaeruminis and C.xerosis.

In an aspect, non-pathogenic microorganism living more than second include it is selected from the group below it is one or more, two kinds or More kinds of, three or more, four kinds or more, five kinds or more, point of six kinds or more or seven kinds or more Ramibacterium species: mycobacterium tuberculosis, M.leprae, M.avium-intracellulare, M.bovis, M.cheloiei、M.africanum、M.marinium、 M.buruli、M.fortuitum、M.haemophilum、 M.intracellulare、M.kansasii、 M.littorale、M.malmoense、M.marianum、M.sinuae、 M.szulgai, and M. ulcerans, M.avium, M.flavascens, M.lepraemurium and M.nicroti.

In an aspect, non-pathogenic microorganism living more than second include it is selected from the group below it is one or more, two kinds or More kinds of, three or more, four kinds or more, five kinds or more, the promise of six kinds or more or seven kinds or more Cattell bacterium strain: N.abscessus, N.acidivorans, N.africana, N.alba, N.altamirensis, N.amamiensis、N.anaemiae、N. aobensis、N.araoensis、N.arthritidis、N.asiatica、 N.asteroides、N.beijingensis、 N.blacklockiae、N.brasiliensis、N.brevicatena、 N.caishijiensis、N. calitrisensis、N.carnea、N.cerradoensis、N.concava、 N.coubleae、N. crassostreae、N.cummidelens、N.cyriacigeorgica、N.elegans、 N.exalbida、N.farcinica、N.flavorosea、N.fluminea、N.gamkensis、N.harensis、N. higoensis、N.ignorata、N.inohanensis、N.iowensis、N.jejuensis、N. jiangxiensis、 N.jinanensis、N.kruczakiae、N.lijiangensis、N.mexicana、 N.miyunensis、 N.neocaledoniensis、N.niigataensis、N.ninae、N.nova、 N.otitidiscaviarum、 N.paucivorans、N.pigrifrangens、N.pneumoniae、N. polyresistens、 N.pseudobrasiliensis、N.pseudovaccinii、N.puris、N. salmonicida、N.seriolae、 N.shimofusensis、N.sienata、N.soli、N.speluncae、 N.takedensis、N.tenerifensis、 N.terpenica、N.testacea、N.thailandica、N. transvalensis、N.uniformis、N.vaccinii、 N.vermiculata, N.veterana, N. vinacea, N.wallacei, N.xishanensis and N.yamanashiensis。

In an aspect, non-pathogenic microorganism living more than second include it is selected from the group below it is one or more, two kinds or It is more kinds of, three or more, four kinds or more, five kinds or more, six kinds or more or seven kinds or more it is red Coccus strain: R.aurantiacus, R.aetherivorans, R.baikonurensis, R.coprophilus, R.corynebacterioides、R.equi、R. erythropolis、R.fascians、R.globerulus、 R.gordoniae、R.imtechensis、R.jostii、 R.koreensis、R.kroppenstedtii、 R.kunmingensis、R.kyotonensis、R. maanshanensis、R.marinonascens、R.opacus、 R.percolatus、R.phenolicus、 R.pyridinivorans、R.qingshengii、R.rhodnii、 R.rhodochrous、R.ruber、 R.triatomae、R.tukisamuensis、R.wratislaviensis、 R.yunnanensis and R. zopfii.

In an aspect, non-pathogenic microorganism living more than second include it is selected from the group below it is one or more, two kinds or More kinds of, three or more, four kinds or more, five kinds or more, six kinds or more or so seven kinds: Skermania piniformis、Williamsia deligens、Williamsia serinedens、Williamsia Maris, Williamsia marianensis, Williamsia muralis and Williamsia faeni.

In an aspect, non-pathogenic microorganism living more than second include it is selected from the group below it is one or more, two kinds or More kinds of, three or more, four kinds or more, five kinds or more, the junket of six kinds or more or seven kinds or more The village Suan Zhong bacterium strain: T.paurometabola, T. spumae, T.inchonensis, T.sunchonensis, T.pseudospumae, T.spongiae, T.pulmonis, T.tyrosinosolvens and T.strandjordii.

Many chronic diseases and enterogastric diseases have chronic infection/infect as its potential pathological condition (for example, bursting Ulcer colitis).In an aspect, the present invention includes and is related to fecal microorganism, one such or multiple-microorganism object Kind, its active fragment or component be used to treat and/or prevent it is various in gastrointestinal tract "abnormal" microbiologic population there are related Morbid state (for example, ulcerative colitis) purposes.The active fragment of bacterium can be by be used to prepare/identify bacterium Any bioactive molecule that any known method of the active fragment of the bacterium and protein of secretion is separated from these bacteriums.In this way Method include but is not limited to: DNA appropriate, detergent cracking, high pressure and is transferred to osmotic shock by ultrasonic treatment Other organisms, such as bacterium, plant or animal, are then used as feed addictive, as previously described.In an aspect, bacterium Active fragment or group be selected from: by mould hydrochlorate or derivatives thereof, polysaccharide, lipopolysaccharides, small peptide, sulphur peptide, protein, nucleic acid point The composition of son, metabolin, cell-wall components or any combination thereof composition.In another aspect, active fragment is secretion egg It is white.

In an aspect, the present disclosure also provides the IBD or other illnesss for treating subject in need Pharmaceutical composition and its method or purposes, wherein the composition includes fecal microorganism preparation, the fecal microorganism system Agent be able to suppress or more than first non-pathogenic microorganisms living of antagonism Fusobacterium species and be able to suppress or antagonism branch More than the second of Bacillus species non-pathogenic microorganism mixing, supplement or enhancing living.In one aspect, fecal microorganism preparation Complete or essentially completed microorganism comprising donor.In one aspect, fecal microorganism preparation includes non-selected excrement Microorganism.On the other hand, fecal microorganism preparation includes separation or purifying work non-pathogenic fecal bacteria group.A side In face, the preparation of fecal microorganism preparation include selected from alcohol treatment, detergent-treatment, heat treatment, radiation, ultrasonic treatment and its Combined processing.In an aspect, the preparation of fecal microorganism preparation is not related to selected from alcohol treatment, detergent processing, heat Processing, radiation and the processing being ultrasonically treated.In an aspect, the preparation of fecal microorganism preparation include selected from filtering, screening, The separating step of density gradient, filtering, chromatography and combinations thereof.In an aspect, the preparation of fecal microorganism preparation does not need Selected from filtering, screening, density gradient, filtering and chromatographic one or more separating steps.In an aspect, the micro- life of excrement Object preparation is substantially free of abitotic substance.In an aspect, fecal microorganism preparation substantially free of selected from residual fibers, The cell-free material of DNA, viral coat material and non-viable bacteria material.In an aspect, fecal microorganism preparation is not substantially Containing the eukaryocyte from the fecal microorganism donor.

In an aspect, the present invention provides treat subject in need illness (for example, ulcerative colitis or Crohn disease) method, wherein this method include to subject apply pharmaceutical activity dosage therapeutic combination, it includes living Non-pathogenic fecal bacteria.In another aspect, this disclosure provides the groups comprising non-pathogenic fecal bacteria living It closes object and is preparing the purposes in the drug for treating illness (for example, ulcerative colitis or Crohn disease).

In an aspect, a method of for treating ulcerative colitis, the ulcerative colitis is selected from ulcer Property rectitis, proctosigmoiditis, left sided colitis and general ulcerative colitis.

In an aspect, therapeutic combination includes the non-pathogenic fecal bacteria group of separation or purifying work.One In a aspect, a kind of therapeutic combination includes non-selected fecal microorganism.In another aspect, therapeutic combination includes not Selection and essentially completed fecal microorganism.In another aspect, therapeutic combination includes full spectrum fecal microorganism.One In a aspect, a kind of method is further comprising administering to 5-aminosalicylic acid agent, corticosteroid, immunosuppressor or combinations thereof.Another In one aspect, a kind of method further comprising administering to 5-aminosalicylic acid or derivatives thereof, sulfasalazine or derivatives thereof or its Combination.

In an aspect, one or more ulcerative colitis symptoms are eliminated or reduced this disclosure provides a kind of Method, the ulcerative colitis symptom be selected from diarrhea, spasm, tenesmus, weight loss, bleeding, loss of appetite, abdomen Bitterly, fever, fatigue, anaemia, inflammation and micro- ulcer.

In an aspect, this disclosure provides the illnesss for the treatment of subject with this need (for example, exedens knot Enteritis or Crohn disease) method, wherein this method include applied to subject pharmaceutical activity dosage comprising non-cause of disease living The therapeutic combination of property bacterium.In an aspect, the present invention provides treatment subject with this need illness (for example, Ulcerative colitis or Crohn disease) method, wherein this method include daily to subject apply pharmaceutical activity dosage packet Therapeutic combination containing non-pathogenic fecal bacteria living.In an aspect, therapeutic combination is at least given once a day Patient with this need is two days at least continuous.In an aspect, at least application is primary daily for therapeutic combination, continue at least 3, 4,5,6,7,8,9,10,11,12,13,14 or 15 days.In another aspect, therapeutic combination is administered at least once daily, It is at least 1,2,3,4,5,6,7,8,9,10,11 or 12 week continuous.In an aspect, therapeutic combination at least application one daily It is secondary, it is continued up to 4,5,6,7,8,9,10,11,12,13,14,15,16,17,18,19 or 20 days or several weeks.In another side In face, therapeutic combination is administered at least once daily, and is continued up to 1,2,3,4,5,6,7,8,9,10,11 or 12 week or several months. On the other hand, therapeutic combination is at least applied once, continues at least 1,2,3,4,5,6,7,8,9,10,11 or 12 months or number Year, chronic administration is in the entire service life of subject or indefinite duration.

In an aspect, it is two days at least continuous that therapeutic combination is given to patient with this need at least twice daily. In an aspect, therapeutic combination is at least applied 2 times daily, continues at least 3,4,5,6,7,8,9,10,11,12,13,14 Or 15 days.In another aspect, therapeutic combination is at least applied 2 times daily, continue at least 1,2,3,4,5,6,7,8,9,10, 11 or 12 weeks.In an aspect, therapeutic combination is at least applied 2 times daily, continue most 4,5,6,7,8,9,10,11, 12,13,14,15,16,17,18,19 or 20 days or week.In another aspect, therapeutic combination is at least applied 2 times daily, is held Continue most 1,2,3,4,5,6,7,8,9,10,11 or 12 weeks or the moon.On the other hand, therapeutic combination is applied at least twice, until Few continuous 1,2,3,4,5,6,7,8,9,10,11 or December or year, chronic administration is in the entire service life of subject or indefinite duration.

In an aspect, it is two days at least continuous that therapeutic combination is given to patient with this need at least three times daily. In an aspect, therapeutic combination is at least applied 3 times daily, continues at least 3,4,5,6,7,8,9,10,11,12,13,14 Or 15 days.In another aspect, therapeutic combination is at least applied 3 times daily, continue at least 1,2,3,4,5,6,7,8,9,10, 11 or 12 weeks.In an aspect, therapeutic combination is at least applied 3 times daily, continue most 4,5,6,7,8,9,10,11, 12,13,14,15,16,17,18,19 or 20 days or week.In another aspect, therapeutic combination is at least applied 3 times daily, is held Continue most 1,2,3,4,5,6,7,8,9,10,11 or 12 weeks or the moon.On the other hand, therapeutic combination is applied at least three times, until Few continuous 1,2,3,4,5,6,7,8,9,10,11 or December or year, chronic administration is in the entire service life of subject or indefinite duration.

In an aspect, this disclosure provides the illnesss for the treatment of subject with this need (for example, exedens knot Enteritis or Crohn disease) method, wherein give subject's therapeutic combination of pharmaceutical activity dosage the method includes oral, The therapeutic combination includes living, nonpathogenic, synthesis bacterial mixture or work, nonpathogenic, purifying or extraction Fecal microorganism, middle dosage apply at least continuous three days or a few weeks with dosage regimen at least one time daily or twice.Another In one aspect, dosage is administered at least once daily, twice or thrice, continues 1 to 12 week, 2 to 12 weeks, 3 to 12 weeks, 4 to 12 Week, 5 to 12 week, 6 to 12 week, 7 to 12 week, 8 to 12 week, 9 to 12 week, 10 to 12 week, 1 to 2 week, 2 to 3 week, 3 to 4 week, 4 to 5 weeks, 5 to 6 weeks, 6 to 7 weeks, 7 to 8 weeks, 8 to 9 weeks, 9 to 10 weeks or 10 to 11 weeks.In another aspect, described herein Dosage is at least one time daily or twice or at least once a week or dosage regimen application at least 3,8,10 or 20 weeks twice. On the other hand, dosage at least one time daily or twice or at least once a week or twice at least 4,5,6,7,11,12,13, 14, dosage regimen application in 15,16,17,18 or 19 weeks.In an aspect, former weeks are continuous weeks.On the other hand In, former weeks are discontinuous weeks.

In an aspect, this disclosure provides the illnesss for the treatment of subject with this need (for example, exedens knot Enteritis or Crohn disease) method, wherein this method includes the first dosage regimen, followed by the second dosage regimen.A side In face, first dosage regimen includes treatment or inductive dose.In an aspect, first dosage regimen includes successive administration Scheme.In another aspect, the second dosage regimen includes the dimension of the pharmaceutical active dosage less than or equal to the first dosage regimen Hold dosage.In another aspect, second dosage regimen continue at least about 2,4,6,8,10,12,18,24,36,48,72 or 96 months.In an aspect, second dosage regimen perennity is applied to the entire service life of treated subject, or The indefinite duration.In an aspect, second dosage regimen is continuous dosing regimens.In another aspect, Two dosage regimens are intermittent dosing regimens.On the other hand, the second dosage regimen is intermittent dosing regimen comprising at least 1, 2,3,4,5,6,7,8,9,10,11,12,13 or 14 days treatment phases, followed by least 1,2,3,4,5,6,7,8,9,10,11, 12,13 or 14 days rest periods.In another aspect, second dosage regimen include every other day, every 2 days or every 3,4, 5, application the second dosage (such as maintenance dose) in 6,7,8 days.In another aspect, maintenance dose be with or without titration (or Otherwise change dosage or dosage regimen) in the case where apply for a long time.In an aspect, first and second prescription is given Interval between case is at least about 1,2,3,4,5,6,7,8,9,10,11 or 12 week.In another aspect, second prescription is given Case (for example, maintenance dose) includes lower than the dosage used in first time dosage regimen (for example, initial treatment dosage) about 2, 5,10,50,100,200,400,800,1000,5000 or more dosage.In another aspect, the second dosage regimen (for example, maintaining dosage regimen) has administration frequency identical or lower with the first dosage regimen (for example, initial treatment is to prescription Case).In another aspect, the second dosage regimen (for example, maintaining dosage regimen) has give more higher than the first dosage regimen Medicine interval (for example, initial treatment dosage regimen).

In an aspect, first or second dosage regimen used in method can be once a week, twice a week or Three-times-weekly.Term " once a week " refers to that dosage application in one week is primary, preferably in application on the same day weekly." weekly Refer to that dosage is administered twice in one week twice ", is preferably administered identical two days weekly." three-times-weekly " refer to dosage one It is administered three times in week, is preferably administered identical three days weekly.

In an aspect, treated subject is to have suffered from illness (for example, ulcerative colitis or Crow grace Disease) subject.It gives disclosed therapeutic combination to inheritance susceptible or is susceptible to suffer from illness (such as ulcerative colitis or Crow Grace disease) asymptomatic human experimenter can also be used for prevention clinical symptoms breaking-out.Inheritance susceptible is susceptible to suffer from ulcerative colitis Human experimenter can be shown with intimate kinsfolk or relatives or with disease (for example, ulcerative colitis Or Crohn disease) human experimenter.In another aspect, treated subject will prevent ulcerative colitis Subject.In another aspect, the subject treated be susceptible to suffer from or be susceptible to suffer from certain disease (for example, ulcerative colitis or gram Sieve grace disease).In another aspect, treated subject be diagnosed as with illness (for example, ulcerative colitis or gram Sieve grace disease) subject.In an aspect, treated subject is patient in need.In another aspect, receive The patient for the treatment of is immunologic hypofunction.

In an aspect, treated subject is human patients.In an aspect, patient is male patient.? In one aspect, patient is female patient.In an aspect, patient is premature.In an aspect, patient is newborn Youngster.In an aspect, patient is newborn.In an aspect, patient is baby.In an aspect, patient is to learn to walk Phase child.In an aspect, patient is child.In an aspect, patient is child.In an aspect, patient is green It is juvenile.In an aspect, patient is pediatric patients.In an aspect, patient is gerontal patient.In an aspect, people Class patient is less than about 18,15,12,10,8,6,4,3,2 or 1 years old child patient.In another aspect, human patients are Adult patients.In another aspect, human patients are gerontal patients.On the other hand, human patients be about 30,35,40, 45,50,55,60,65,70,75,80,85,90 or 95 years old or more patient.In another aspect, patient age is about 1 Between to 5, between 2 to 10, between 3 to 18, between 21 to 50, between 21 to 40, between 21 to 30, between 50 to 90,60 arrive Between 90, between 70 to 90 years old, between 60 to 80 years old or between 65 to 75 years old.In an aspect, patient is one young Patient (65-74 years old).In an aspect, patient is aged patients (75-84 year old).In an aspect, patient is one old Year patient (> 85 years old).

In an aspect, a kind of method includes oral, bowel lavage or gives therapeutic combination by rectal suppository.At one In aspect, the therapeutic combination being administered herein is configured to enteric coated capsule or microcapsules, acidproof capsule or microcapsules, or with Food, food additives, dairy products, soybean base product or derivatives thereof, jelly, seasoned liquid, ice cube, ice cream or Yoghourt one It rises and prepares or apply together.In another aspect, the therapeutic combination applied herein is formulated as to acidproof enteric coating glue Capsule.In another aspect, the therapeutic combination applied herein is configured to the capsule of dual encapsulating.Therapeutic combination can be made It is provided to combine the powder sold with food or beverage.Food or beverage can be product based on dairy products or based on soybean Product.In another aspect, food or food supplement include the enteric coating containing therapeutic combination and/or acidproof micro- glue Capsule.

In one aspect, therapeutic combination includes liquid culture.In another aspect, therapeutic combination is lyophilized, Crush simultaneously dusting.Then it can be injected into, be dissolved in such as salt water, as enema.Alternatively, can be intestines by powder coating Molten coating and/or acidproof capsule, for being administered orally.These capsules can be using the shape of enteric coating and/or acidproof microcapsules Formula.Powder is preferably provided in palatable form, is drunk for reconstructing or is reconstructed as food additives.On the other hand, it eats Object is Yoghourt.In an aspect, powder can be rebuild by nose-duodenum infusion to be transfused.

In another aspect, the therapeutic combination being administered herein is liquid, freezing, freeze-drying, foam-drying, is sprayed Dry, freeze-drying or powder type.On the other hand, the therapeutic combination applied herein is formulated as delay or gradual enteric release Form.In another aspect, therapeutic combination given herein includes excipient, salt water, buffer, buffer or fluid- Glucose-cellobiose agar (RGCA) culture medium.In another aspect, therapeutic combination given herein includes that freezing is protected Protect agent.In an aspect, a kind of cryoprotector includes polyethylene glycol, skimmed milk, antierythrite, arabite, sorb Sugar alcohol, glucose, fructose, alanine, glycine, proline, sucrose, lactose, ribose, trehalose, dimethyl sulfoxide (DMSO), Glycerol or combinations thereof.

In an aspect, the therapeutic combination given herein also includes acid inhibitor, antiacid, H2 antagonist, proton Pump inhibitor or combinations thereof.In an aspect, therapeutic combination given herein is substantially free of abitotic substance.Another In a aspect, the therapeutic combination given herein is substantially free of selected from remnant fibrous, DNA, viral coat material and non-viable bacteria The cell-free material of material.

In an aspect, therapeutic combination also includes or is supplemented with prebiotic nutrescin selected from the group below: polyalcohol, low Fructooligosaccharides (FOS), oligofructose, inulin, galactooligosaccharide (GOS), xylo-oligosaccharide (XOS), polydextrose, monosaccharide, Tagatose, And/or manna oligosacchride.

In an aspect, this method further includes using antibiotic before application therapeutic bacterial or micropopulation composition Composition pre-processes subject.In an aspect, antibiotic composition given herein includes antibiotic selected from the group below: benefit Fu Buting, clarithromycin, Clofazimine, vancomycin, rifampin, nitroimidazole, chloramphenicol and combinations thereof.On the other hand In, antibiotic composition given herein include antibiotic selected from the group below: rifaximin, Ryfamycin derivative, rifampin, Rifabutin, Rifapentine, rifalazil, than Ka-7038Ⅶ, aminoglycoside, gentamicin, neomycin, streptomysin, paromomycin, Verdamicin, mutamicin, sisomicin, Netilmicin, retymicin, kanamycins, aztreonam, rheum emodin, big ring Lactone, clarithromycin, Dirithromycin, roxithromycin, Ketek, azithromycin, bismuth subsalicylate, vancomycin, streptomysin, Feldamycin, amikacin, Arbekacin, neomycin, Netilmicin, paromomycin, red streptomysin, tobramycin, An Pu Mycin and combinations thereof.On the other hand, a kind of method further includes using before application therapeutic bacterial or micropopulation composition Anti-inflammatory agent pre-processes subject.In another aspect, antibiotic includes by Amoxicillin, tetracycline and metronidazole (ATM) group At antibiotic combinations scheme.See, for example, Kato et al., Aliment Pharmacol Ther 39:949-56 (2014)； Koido et al., PLOS One, 9 (1): e86702 (2014)；Nitzan et al., World J Gastroenterol. 22 (3): 1078–87(2016)。

In an aspect, a kind of method realizes alleviation, healing, reaction or the extinction rate of ulcerative colitis at least about 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 97% or 99%.In an aspect, a kind for the treatment of method reaches ulcerative colitis after treatment 8 weeks Scorching disease activity index (UCDAI) reduces by more than 2,3,4,5,6,7,8,9,10 or 11.In other side, a kind for the treatment of method Treatment 8 weeks after reach ulcerative colitis disease activity index (UCDAI) PATIENT POPULATION at least 10%, 20%, 30%, it reduces more than 2,3,4,5,6,7,8,9,10 or 11 in 50%, 60%, 70%, 80% or 90%.In an aspect, Compared with baseline (for example, before the treatment), after treatment 8 weeks, treatment method can make ulcerative colitis disease activity index (UCDAI) at least 10%, 20%, 30%, 50%, 60%, 70%, 80% or 90% is reduced.In an aspect, with baseline phase Than (for example, before treatment), after treatment 8 weeks, treatment method at least 10%, 20%, 30%, 50%, 60%, 70%, Can make in 80% or 90% patient ulcerative colitis disease activity index (UCDAI) reduce at least 10%, 20%, 30%, 50%, 60%, 70%, 80% or 90%.

On the other hand, patient, such as Schroeder are assessed using disease activity index (DAI) or Mayo points-scoring system People is in Coated oral 5-aminosalcylic acid therapy for mildly to moderately active ulcerative colitis.N Eng J Med.1987；Described in 317:1625-1629.In an aspect, with baseline Compare, after treatment 8 weeks, treatment method reach Mayo scoring at least 10%, 20%, 30%, 50%, 60%, 70%, 80% or 90% reduction (for example, before the treatment).In an aspect, it compared with baseline (for example, before treatment), controls Treatment method can make Mayo scoring after treatment 8 weeks at least 10%, 20%, 30%, 50%, 60%, 70%, 80% or Reduce by least 10%, 20%, 30%, 50%, 60%, 70%, 80% or 90% in 90% patient.

In an aspect, the pharmaceutical composition of every about 200mg includes pharmacological activity dosage.In an aspect, often The drug of about 75,100,125,150,175,200,250,300,350,400,450,500,750,1000,1500 or 2000mg Composition includes pharmacological activity dosage.

In an aspect, pharmaceutical active or treatment effective dose include at least about 10⁵、10⁶、10⁷、 10⁸、10⁹、10¹⁰、 10¹¹、10¹²、10¹³、10¹⁴Or 10¹⁵cfu.In another aspect, pharmaceutical active treatment effective dose includes at most about 10⁵、 10⁶、10⁷、10⁸、10⁹、10¹⁰、10¹¹、10¹²、 10¹³、10¹⁴Or 10¹⁵cfu.On the other hand, pharmacological activity treats effective agent Amount is selected from: 10⁸cfu-10¹⁴cfu、10⁹cfu-10¹³cfu、10¹⁰cfu-10¹²cfu、10⁹cfu-10¹⁴cfu、 10⁹cfu- 10¹²cfu、10⁹cfu-10¹¹cfu、10⁹cfu-10¹⁰cfu、10¹⁰cfu-10¹⁴cfu、 10¹⁰cfu-10¹³cfu、10¹¹cfu- 10¹⁴cfu、10¹¹cfu-10¹³cfu、10¹²cfu-10¹⁴Cfu and 10¹³cfu-10¹⁴cfu.In an aspect, pharmaceutical composition It is about 0.2,0.4,0.6,0.8 or 1.0 gram or unit volume comprising foregoing pharmaceutical activity or treatment effective dose, Unit Weight It is about 0.2,0.4,0.6,0.8 or 1.0 milliliter.

In an aspect, pharmaceutical active or treatment effective dose include at least about 10⁵、10⁶、10⁷、 10⁸、10⁹、10¹⁰、 10¹¹、10¹²Or 10¹³A cell or spore.In another aspect, pharmaceutical active or treatment effective dose include at most about 10⁵、 10⁶、10⁷、10⁸、10⁹、10¹⁰、10¹¹、10¹²Or 10¹³A total cell or spore.On the other hand, pharmacological activity or treatment have Effect dosage is selected from: 10⁸-10¹⁴、10⁹-10¹³、10¹⁰-10¹²、10⁹-10¹⁴、10⁹-10¹²、10⁹-10¹¹、10⁹-10¹⁰、10¹⁰-10¹⁴、 10¹⁰-10¹³、10¹¹-10¹⁴、10¹¹-10¹³、10¹²-10¹⁴With 10¹³-10¹⁴Cell or spore.In one aspect, it pharmaceutical active or controls It treats effective dose cell count and is directed to living cells.In an aspect, pharmaceutical composition includes that said medicine activity or treatment have Dosage is imitated, Unit Weight is about 0.2,0.4,0.6,0.8 or 1.0 gram or unit volume is about 0.2,0.4,0.6,0.8 or 1.0 Milliliter.In one aspect, pharmaceutical active or treatment effective dose include 10¹⁰To 10¹²A cell.In another aspect, drug Activity or treatment effective dose include each capsule 10¹⁰To 10¹²A cell.

In an aspect, the therapeutic combination applied herein includes fecal bacteria.In an aspect, given herein Therapeutic combination include it is selected from the group below it is one or more, two or more, it is three or more, four kinds or more or Five kinds or more separation, purifying or culture microorganisms: clostridium, Bacillus, Collins Salmonella, Bacteroides, Eubacterium, Fusobacterium, Propionibacterium, lactic acid bacteria, Ruminococcus, Escherichia coli, Gemmiger, Desulfomonas, Pepto streptococcus, Bifidobacterium, fecal bacteria, Dorea and Monilia.

In an aspect, fecal microorganism preparation as described herein includes the fecal bacteria mixture of purifying or reconstruct. In an aspect, fecal microorganism preparation include it is selected from the group below it is one or more, two or more, it is three kinds or more Kind, four kinds or more or five kinds or more Fecal organisms living: amino acid coccus, Ackermam bacterium, Alistipes, Anaerotruncus, Bacteroides, Bifidobacterium, Blaw spy Salmonella, Butyrivibrio, clostridium, Collins Salmonella, excrement ball Bacterium, corynebacteria, Dorea, enterococcus, Escherichia, Eubacterium, pula clostridium bacterium, haemophilus, Holdemania, lactic acid Bacterium, catarrhalis, Parabacteroides, Prey irrigate bacterium, Propionibacterium, Raoul bacterium, caecum Ross Salmonella, Ruminococcus, Staphylococcus, streptococcus, rare micrococcus and Veillonella.In an aspect, fecal microorganism preparation includes and is selected from the group It is one or more, two or more, three or more, four kinds or more or five kinds or more Fecal organisms living: Bacteroides fragilis ssp.vulgatus, Collins Salmonella aerofaciens, Bacteroides fragilis Ssp. thetaiotaomicron, Pepto streptococcus productus II, Parabacteroides distasonis, pula Clostridium, fecal bacteria eutactus, Pepto streptococcus productus, Ruminococcus bromii, Bifidobacterium adolescentis, Gemmiger formicilis, Bifidobacterium longum, Eubacterium siraeum, Ruminococcus torques, Eubacterium Rectale, Eubacterium eligens, Bacteroides eggerthii, clostridium leptum, Bacteroides fragilis Ssp.A, Eubacterium biforme, Bifidobacterium infantis, Eubacterium rectale, fecal bacteria comes, Pseudoflavonifractor capillosus, Ruminococcus albus, Dorea formicigenerans, Eubacterium Hallii, Eubacterium ventriosum, Russian Fusobacterium, Ruminococcus obeum, Eubacterium rectale, clostridium Ramosum, lactic acid bacteria leichmannii, Ruminococcus callidus, Butyrivibrio crossotus, amino acid coccus Fermentans, Eubacterium ventriosum, Bacteroides fragilis ssp. fragilis, fecal bacteria catus, Aerostipes hadrus, Eubacterium cylindroides, Eubacterium ruminantium, staphylococcus epidermidis, Eubacterium limosum, Tissirella praeacuta, Fusobacterium mortiferum, Fusobacterium Naviforme, clostridium innocuum, clostridium ramosum, Propionibacterium acnes, Ruminococcus flavefaciens, Bacteroides fragilis ssp.ovatus、Fusobacterium nucleatum、Fusobacterium Mortiferum, Escherichia coli, Gemella morbillorum, Finegoldia magnus, streptococcus Intermedius, Ruminococcus lactaris, Eubacterium tenue, Eubacterium ramulus, Bacteroides Clostridiiformis ssp.clostridliformis, Bacteroides coagulans, Prey irrigate bacterium oralis, general Thunder irrigates bacterium ruminicola, Odoribacter splanchnicus and Desuifomonas pigra.

In an aspect, fecal microorganism preparation lack or substantially free of it is selected from the group below it is one or more, two kinds Or a variety of, three or more, four kinds or more or five kinds or more fecal microorganisms living: amino acid coccus, Ackermam Bacterium, Alistipes, Anaerotruncus, Bacteroides, Bifidobacterium, Blaw spy Salmonella, Butyrivibrio, clostridium, Ke Woods this Salmonella, fecal bacteria, corynebacteria, Dorea, enterococcus, Escherichia, Eubacterium, pula clostridium bacterium, haemophilus, Holdemania, lactic acid bacteria, catarrhalis, Parabacteroides, Prey irrigate bacterium, Propionibacterium, Raoul bacterium, caecum sieve This Salmonella, Ruminococcus, staphylococcus, streptococcus, rare micrococcus and Veillonella.In an aspect, fecal microorganism Preparation lack or substantially free of it is selected from the group below it is one or more, two or more, it is three or more, four kinds or more Kind or five kinds or more of fecal microorganism: Bacteroides fragilis ssp.vulgatus, Collins Salmonella Aerofaciens, Bacteroides fragilis ssp.thetaiotaomicron, Pepto streptococcus productus II, Parabacteroides distasonis, pula clostridium, fecal bacteria eutactus, Pepto streptococcus productus, Ruminococcus bromii, Bifidobacterium adolescentis, Gemmiger formicilis, Bifidobacterium longum, Eubacterium Siraeum, Ruminococcus torques, Eubacterium rectale, Eubacterium eligens, Bacteroides eggerthii, shuttle Bacterium leptum, Bacteroides fragilis ssp. A, Eubacterium biforme, Bifidobacterium infantis, Eubacterium Rectale, fecal bacteria comes, Pseudoflavonifractor capillosus, Ruminococcus albus, Dorea Formicigenerans, Eubacterium hallii, Eubacterium ventriosum, Russian Fusobacterium, Ruminococcus obeum, true bar Bacterium rectale, clostridium ramosum, lactic acid bacteria leichmannii, Ruminococcus callidus, Butyrivibrio crossotus, Amino acid coccus fermentans, Eubacterium ventriosum, Bacteroides fragilis ssp.fragilis, excrement ball Bacterium catus, Aerostipes hadrus, Eubacterium cylindroides, Eubacterium ruminantium, staphylococcus Epidermidis, Eubacterium limosum, Tissirella praeacuta, Fusobacterium mortiferum, Fusobacterium naviforme, clostridium innocuum, clostridium ramosum, Propionibacterium acnes, Ruminococcus flavefaciens、 Bacteroides fragilis ssp.ovatus、Fusobacterium nucleatum、 Fusobacterium mortiferum, Escherichia coli, Gemella morbillorum, Finegoldia magnus, Streptococcus intermedius, Ruminococcus lactaris, Eubacterium tenue, Eubacterium ramulus, Bacteroides Clostridiiformis ssp.clostridliformis, Bacteroides coagulans, Prey irrigate bacterium oralis, general Thunder irrigates bacterium ruminicola, Odoribacter splanchnicus and Desuifomonas pigra.

In an aspect, therapeutic combination given herein includes fecal microorganism.In another aspect, make herein The preparation of fecal microorganism be related to selected from alcohol treatment, detergent-treatment, heat treatment, radiation and ultrasonic treatment processing. In another aspect, the preparation of fecal microorganism used herein does not include selected from alcohol treatment, detergent-treatment, Re Chu Reason, radiation and the processing being ultrasonically treated.In an aspect, the preparation of fecal microorganism used herein includes being selected from density level bands Degree, filtering (such as sieve, nylon wire) and chromatographic separating step.In another aspect, the micro- life of excrement used herein The preparation of object does not include selected from density gradient, filtering (such as sieve, nylon wire) and chromatographic separating step.On the other hand In, fecal microorganism used herein includes the entire fecal microorganism of donor.In another aspect, the treatment given herein Composition includes the fecal microorganism substantially free of the eukaryocyte from fecal microorganism donor.

In another aspect, the therapeutic combination being administered herein includes further to supplement, mix or use fecal microorganism The fecal microorganism of enhancing.In an aspect, fecal microorganism be supplemented with clostridium, Collins Salmonella, Dorea, Ruminococcus, Fecal bacteria, Prey irrigate bacterium, Veillonella, Bacteroides, Baccillus or combinations thereof non-pathogenic (or pathogenicity subtracts Poison) bacterium.In another aspect, the therapeutic combination given herein includes fecal microorganism, further uses Wei Rongqiu Bacterium ceae, Firmicutes, Gammaproteobacteria, Bacteroidetes or combinations thereof strain supplement, incorporation increase By force.In another aspect, the therapeutic combination given herein includes the micro- life of excrement for being further supplemented with fecal bacteria spore Object.In an aspect, fecal bacteria spore is clostridium spore, subtilis spore or both.

In one aspect, therapeutic combination include the fecal microorganism from subject, the subject be selected from people, ox, Cow calf, ruminant, sheep, goat or deer.In another aspect, therapeutic combination can be applied to selected from people, ox, cream The subject of calf, ruminant, sheep, goat or deer.In one aspect, therapeutic combination substantially or nearly odorlessness.

In one aspect, provided herein is or application therapeutic combination include fecal microorganism, it includes be greater than or equal to 0.3, it is greater than or equal to 0.4, is greater than or equal to 0.5, is greater than or equal to 0.6, is greater than or equal to 0.7, is greater than or equal to 0.8, is big In or equal to 0.9, more than or equal to 1.0, more than or equal to 1.1, more than or equal to 1.2, more than or equal to 1.3, be greater than or wait In 1.4, be greater than or equal to 1.5, be greater than or equal to 1.6, being greater than or equal to 1.7, being greater than or equal to 1.8, being greater than or equal to 1.9, More than or equal to 2.0, more than or equal to 2.1, more than or equal to 2.2, more than or equal to 2.3, more than or equal to 2.4, be greater than or Equal to 2.5, more than or equal to 3.0, more than or equal to 3.1, more than or equal to 3.2, more than or equal to 3.3, be greater than or equal to 3.4, it is greater than or equal to 3.5, is greater than or equal to 3.6, is greater than or equal to 3.7, is greater than or equal to 3.8, is greater than or equal to 3.9, is big In or equal to 4.0, more than or equal to 4.1, more than or equal to 4.2, more than or equal to 4.3, more than or equal to 4.4, be greater than or wait In the 4.5, Shannon diversity index more than or equal to 5.0.In another aspect, therapeutic combination includes fecal microorganism, It includes 0.1-3.0,0.1-2.5,0.1-2.4,0.1-2.3,0.1-2.2,0.1-2.1,0.1-2.0,0.4-2.5,0.4- 3.0、0.5-5.0、0.7-5.0、0.9-5.0、1.1-5.0、1.3-5.0、1.5-5.0、1.7-5.0、 1.9-5.0、2.1-5.0、 2.3-5.0,2.5-5.0,2.7-5.0,2.9-5.0,3.1-5.0,3.3-5.0,3.5-5.0,3.7-5.0,31.9-5.0 or The Shannon diversity index of 4.1-5.0.In an aspect, Shannon diversity index is in door level calculation.On the other hand In, Shannon diversity index is calculated in family's level.In an aspect, Shannon diversity index is belonging to level calculation.Another In one aspect, Shannon diversity index calculates on species level.On the other hand, therapeutic combination includes proportional amount Galenical is similar to the human feces flora of normal health.

On the other hand, therapeutic combination includes the excrement from least 1,2,3,4,5,6,7,8,9 or 10 different family Just bacterium.In another aspect, therapeutic combination includes to come from least 11,12,13,14,15,16,17,18,19 or 20 The fecal bacteria of different families.On the other hand, therapeutic combination include from least 21,22,23,24,25,26,27,28, The fecal bacteria of 29 or 30 different families.On the other hand, therapeutic combination include from least 31,32,33,34,35, 36, the fecal bacteria of 37,38,39 or 40 different families.In another aspect, therapeutic combination include from least 41, 42, the fecal bacteria of 43,44,45,46,47,48,49 or 50 different families.In another aspect, therapeutic combination packet Fecal bacteria containing 1 to 10,10 to 20,20 to 30,30 to 40,40 to 50 different family.In one aspect, provided herein is Or the therapeutic combination of application includes fecal microorganism, it includes no more than 0.05%, 0.1%, 0.2%, 0.3%, 0.4%, 0.5%, 0.6%, 0.7%, 0.8%, 0.9%, 1%, 2%, 3%, 4%, 5%, 6%, 7%, 8%, 9% or 10% weight Non-biological material/weight biomaterial.In another aspect, provided herein is or application therapeutic combination include excrement it is micro- Biology, it includes no more than 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, the non-biological material of 80%, 85%, 90% or 95% weight/weight biomaterial.In another aspect, it mentions herein For or the therapeutic combination of application include non-biological material particle by the fecal specimens of sieve, pillar or similar filter device And/or particles of bioglass；By the fecal specimens by sieve, pillar or similar filter device non-biological material particle and/ Or particles of bioglass forms or substantially by the non-biological material of the fecal specimens by sieve, pillar or similar filter device Particle and/or particles of bioglass composition, the similar filter device with having a size of 2.0mm, 1.0mm, 0.5mm, 0.25mm, 0.212mm、0.180mm、0.150mm、 0.125mm、0.106mm、0.090mm、0.075mm、0.063mm、0.053mm、 Sieve, tap or the particle mistake of 0.045mm, 0.038mm, 0.032mm, 0.025mm, 0.020mm, 0.01mm or 0.002mm Filter." nonliving material " does not include excipient, such as the pharmaceutical inert substance being added in finished fecal material is for example Cryoprotector." biomaterial " refers to the living materials in excrement, and the microorganism including such as prokaryotic cell, such as carefully Bacterium and archeobacteria (such as prokaryotic cell living and spore can be formed to become the spore of prokaryotic cell living)；Eukaryocyte, Such as protozoan and fungi；And virus.In one embodiment, " biomaterial " refers to the colon for being present in normal healthy people In living materials, such as microorganism, eukaryocyte and virus.In one aspect, provided herein is or application therapeutic combination Comprising human faecal mass extract, wherein composition substantially odorlessness.In one aspect, provided herein is or application therapeutic combination Include the fecal materials or excrement flower preparation in freeze-drying, crude, half purifying or pure preparations.

In one aspect, the fecal microorganism in therapeutic combination includes highly purified or purifying faecal microbiota, for example, Substantially free of non-colored fecal materials.In one aspect, can before screening, after or before and be further processed excrement later Just microorganism (for example, by carrying out micro-filtration).In another aspect, highly purified fecal microorganism product is by ultrafiltration to remove It goes macromolecular but retains therapeutic micropopulation, such as bacterium.

It in one aspect, include that sterile excrement filtrate or acellular excrement are filtered for the therapeutic combination for the treatment of disclosed herein Liquid.In an aspect, sterile faeces filtrate comes from donor excrement.In another aspect, sterile faeces filtrate is from culture Microorganism.In another aspect, sterile excrement filtrate includes the non-particulate excrement component of acellular.In an aspect, such as Sterile excrement filtrate is prepared described in WO2014/078911 disclosed on May 30th, 2014.In another aspect, in such as Ott Et al. Gastroenterology 152:799-911 (2017) is described prepares sterile excrement filtrate.

In an aspect, filtrate of dejecta includes the secretion of micropopulation, secretion or other liquid components, such as raw Object bioactive molecule (BAM), can be antibiotic or anti-inflammatory agent, saves, retains or reconstructs in flora extract.A side In face, BAM is small RNA molecular, such as siRNA (siRNA), short hairpin RNA (shRNA), trans-acting siRNA (ta- ) or microRNA (miRNA) siRNA.In another aspect, BAM is " non-coding RNA molecule ", is not coding protein RNA molecule.The non-limiting embodiment of non-coding RNA molecule includes Microrna (miRNA), miRNA precursor, siRNA (siRNA), siRNA precursor, tiny RNA (length 18-26nt) and the identical precursor of coding, heterochromatin siRNA (hc- SiRNA), Piwi interaction RNA (piRNA), hair clip double-stranded RNA (hair clip dsRNA), trans-acting siRNA (ta- SiRNA), naturally occurring antisense siRNA (nat-siRNA), CRISPR RNA (crRNA), tracer RNA (tracrRNA), refer to Lead RNA (gRNA) and single guide RNA (sgRNA).

In an aspect, exemplary treatment composition includes the starting material from the donor from restriction donor reservoir, Wherein the donor provides the excrement of centrifugation, is then carried out using metal screening or Millipore filter or equivalent very high Horizontal Filtration Filtration finally only allows the cell of bacterial origin to retain, such as general diameter is less than about 5 microns of cell.? After initial centrifugation, solid material is separated with liquid, then be gradually reduced size filter and tangential flow filtration device (for example, Filtered using Millipore) in cross filter solid, further include using nano-film filtration and optionally.Filtering can also pass through Sieve described in WO2012/122478 carries out, but also using 0.0120mm is less than, down to the sieve of about 0.0110mm, this is most Lead to that there is only bacterial cells eventually.

The supernatant separated in centrifugal process is taken out now, and in filtering (for example, Millipore filtering or equivalent system System) in gradually filter, finally obtain liquid, which passes through about 0.22 micron of filter fine filtering.This can remove all Particulate matter, including all biologies, such as bacterium and virus.Then the product is sterile, but purpose is to retain its secretion While remove bacterium, especially antibacterial bacteriocin, the cytokine-like product of bacterial derivation and all adjoint bioactivity Molecule (BAM), comprising: thuricin (by donor excrement bacillus secrete), bacteriocin (including colicine, Troudulixine or putaindicine or microcin or subtilosinA), lanbiotics it is (including streptococcus lactis peptide, withered Straw mycoproteinase, epidermal protein, mutacin, mersacidin, actagardine and cinnamycin), lactic acid and other Antibacterial or anti-inflammatory compound.In an aspect, therapeutic combination used herein includes that the cell-free excrement rich in bacteriophage is filtered Liquid.In an aspect, lytic phage is enriched with.In another aspect, mild bacteriophage enrichment.In one aspect In, bacteriophage comes from Caudovirales.In another aspect, bacteriophage comes from Ligamenvirales.In one aspect In, bacteriophage comes from family selected from the group below: myopathy poison, siphovirus, podovirus, Lipothrixviridae, ancient phagocytosis Body, Ampullaviridae, Bicaudaviridae, Clavaviridae, Corticoviridae, Cystoviridae, Fuselloviridae、Globuloviridae、 Guttaviridae、Inoviridae、Leviviridae、 Microviridae, Plasmaviridae and Tectiviridae.

In an aspect, therapeutic combination used herein include from it is one or more, 2 or more, 3 or More, 4 or more, 5 or more, the phagocytosis of 6 or more or 7 or more families selected from the group below The combination of body: myopathy poison, siphovirus, podovirus, Lipothrixviridae, ancient bacteriophage, Ampullaviridae, Bicaudaviridae、 Clavaviridae、Corticoviridae、Cystoviridae、Fuselloviridae、 Globuloviridae、 Guttaviridae、Inoviridae、Leviviridae、Microviridae、 Plasmaviridae and Tectiviridae.

In an aspect, therapeutic combination used herein includes the faecal microbiota rebuild, substantially by purifying The group of fecal microorganism and acellular excrement filtrate is combined into.In another aspect, therapeutic combination used herein includes to mend Purifying fecal microorganism filled with the non-particulate excrement ingredient of one or more acellulars.In an aspect, used herein to control Treating composition includes the non-particulate excrement ingredient of one or more acellulars.In an aspect, non-of one or more acellulars It includes synthetic molecules, the bioactive molecule generated by fecal microorganism, or both that pellet, which becomes point,.In another aspect, One or more non-particulate excrement components of acellular include biological activity protein or peptide, micronutrient, fat, sugar, small carbon Hydrate, microelement, mineral salt, ash content, mucus, amino acid, nutrient, vitamin, minerals or any combination thereof.? In one aspect, one or more non-particulate excrement components of acellular include one or more selected from bacteriocin, alkaloid and cream The bioactive molecule of acid.In another aspect, the non-particulate excrement ingredient of one or more acellulars includes one or more Selected from colicine, duodenum glycosides, putaindicine, microcin and subtilisin A bacteriocin.In one aspect In, one or more non-particulate excrement components of acellular include one or more selected from thuricin, streptococcus lactis peptide, hay bacillus Protease, epidermal protein, the lambert of mutacin, mersacidin, actagardine and cinnamycin are biological.Another In a aspect, one or more non-particulate excrement components of acellular include anti-spore compound, Antimicrobe compound, anti-inflammatoryization Close object or any combination thereof.On the other hand, the non-particulate excrement component of one or more acellulars includes interleukins, cell The factor, leukotriene, eicosanoid or any combination thereof.

In another aspect, treatment method provided herein includes using fecal bacteria cell, such as people GI enterobacteria Partly or completely integral representation and plant (micropopulation) separation, processing, filtering, concentration, reconstruct and/or Artificial liquid component (such as excrement filtrate), the plant (micropopulation) includes bacterial secretory product, as bacteriocin (is produced by bacterium Raw archon, the bacterium include colicine, duodenum glycosides or putaindicine or microcin or withered grass Bacteriolysin A), (a kind of peptide antibiotic contains the polycyclic thioether amino acid of characteristic, lanthionine or methyl wool sulphur to alkaloid Propylhomoserin, unsaturated amino acid dehydroalanine and 2- aminoisobutyric acid comprising thuricin is (by the bacillus in donor excrement Secretion), streptococcus lactis peptide, subtilopeptidase A, epidermal protein, mutacin, mersacidin, actagardine, Cinnamycin), lactic acid (a kind of Peptide toxin of pore-forming) and other antimicrobial or anti-inflammatory compounds and/or by micropopulation Bacterium or other microorganisms generate and/or micropopulation " liquid component " in find other biological activities molecule (BAM)。

In an aspect, the therapeutic combination of the therapeutic combination based on fecal bacteria and the acellular filtrate based on excrement Object uses simultaneously.In another aspect, before giving second of therapeutic combination based on fecal bacteria, with the first base Patient is treated in the therapeutic combination of excrement acellular filtrate, vice versa.On the other hand, treatment method includes three steps It is rapid: firstly, antibiotic pretreatment is non-selectively to remove infectious pathogen；Second, the acellular filtrate based on excrement Processing step, to further suppress selected infectious pathogen；Third provides the therapeutic combination based on fecal bacteria to patient Object is with Reconstruction of The Function enteric microorganism group.

In another aspect, the fecal microorganism in therapeutic combination used herein includes or substantially by substantially Separation or purifying faecal microbiota or entire (or essentially completed) micropopulation composition, it is described entire (or substantially complete It is whole) micropopulation be (or comprising) faecal microbiota isolate, the faecal microbiota at least about 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, 99.5%, 99.6%, 99.7%, 99.8% or 99.9% is separation Or it is pure, or have no more than about 0.1%, 0.2%, 0.3%, 0.4%, 0.5%, 0.6%, 0.7%, 0.8%, 0.9% or 1.0% or more non-excrement floral material；Alternatively, if Sadowsky et al. is described in WO2012/122478A1 Or substantially separate, purifying or substantially entire micro- life such as Borody et al. described in WO2012/016287A2 Object group.

In one aspect, the fecal microorganism in therapeutic combination includes the substantially all or non-selected excrement of donor The fecal material of microorganism, the fecal material of reconstruction or synthesis.In another aspect, the fecal microorganism in therapeutic combination Not comprising antibiotic resistance group.In another aspect, therapeutic combination is comprising fecal microorganism and substantially free of outer Come substance (e.g., including the non-living matter of cell-free substance such as residual fibers, DNA, RNA, viral coat material, it is infeasible Raw material, eukaryocyte of the living matter for example from fecal materials donor).

In one aspect, the fresh homologous excrement that the fecal microorganism in therapeutic combination used herein is screened from disease Just or the excrement of equivalent freeze-drying and reconstruct.In one aspect, fresh homologous excrement does not include antibiotic resistance group. In another aspect, the fecal microorganism in therapeutic combination is derived from synthesis excrement composition.In one aspect, excrement is synthesized Just composition includes living flora preparation, similar to normal healthy people faecal microbiota, and does not include resisting preferably with proportional amount Raw element resistance populations.Suitable microorganism can be selected from following: Bacteroides, Eubacterium, Fusobacterium, propionic acid bar Bacterium, lactic acid bacteria, Ruminococcus, Escherichia coli, Gemmiger, clostridium, Desulfomonas, Pepto streptococcus, bifid Bacillus, Collins Salmonella, fecal bacteria, Dorea and Ruminococcus.

In one aspect, therapeutic combination is combined with other adjuvants such as antiacid to inhibit the bacteria inactivation (example in stomach Such as, Mylanta, Mucaine, Gastrogel).It in another aspect, can also using H2- antagonist or proton pump inhibitor Pharmacologically to inhibit the acid secretion in stomach.Embodiment H2- antagonist is ranitidine.Embodiment proton pump inhibitor is Omeprazole.In an aspect, acid inhibitor is applied before applying or being co-administered with therapeutic combination.

In one aspect, the form of therapeutic combination are as follows: coloclysis composite can be reconstructed with suitable diluent；Intestines Colloidal sol capsule；Enteric microcapsule；Acidproof；Acidproof capsule；Acidproof microcapsules；The powder rebuild with appropriate diluent is used for nose intestines Infusion or Sigmoidoscope infusion；The powder for being orally ingested is rebuild with diluent appropriate, flavoring agent and acid inhibitor；With food The powder that object or beverage are rebuild；Or the food of the enteric coating and/or acidproof microcapsules comprising composition, powder, jelly or liquid Product or food supplement.

In one aspect, treatment method realization healing, symptom mitigation or disease symptoms (such as IBD, such as ulcerative colitis Scorching or Crohn disease) percentage reduce.The variation of flora is preferably as far as possible " close to complete ", and the life that flora is lived Object replaces, these organisms will squeeze out any remaining primordial plant group.In general, the variation of intestinal flora includes will be a series of Predetermined microflora introduces gastronintestinal system, therefore in a preferred form, and treatment method includes basic in the patient for needing this treatment Upper or complete displacement Pathogenic enteric flora.

In another aspect, therapeutic combination can provide together with pharmaceutically acceptable carrier.As used herein, " pharmaceutically acceptable carrier " refers to innoxious solvent, dispersing agent, excipient, adjuvant or the other materials mixed with bacterium living, Pharmaceutical composition is formed to allow, for example, the dosage form of patient can be given.Pharmaceutically acceptable carrier can be liquid (example Such as salt water), diluent, adjuvant, excipient or the acidproof encapsulating ingredient of gel or solid form.Suitable diluent and figuration Agent includes physiological saline, dextrose, glycerol, mannitol, lactose, starch, magnesium stearate, saccharin sodium, cellulose, the carbon of pharmaceutical grade Sour magnesium etc. and their combination.In another aspect, therapeutic combination can contain auxiliary substance, such as wetting agent or cream Agent or stabilizer or pH buffer.In one aspect, therapeutic combination contain about 1%-5%, 5%-10%, 10%-15%, 15-20%, 20%-25%, 25-30%, 30-35%, 40-45%, 50%-55%, 1%-95%, 2%-95%, 5%- 95%, 10%-95%, 15%-95%, 20%-95%, 25%-95%, 30%-95%, 35%-95%, 40%-95%, 45%-95%, 50%-95%, 55%-95%, 60%-95%, 65%-95%, 70%-95%, 45%-95%, 80%- The active constituent of 95% or 85%-95%.In one aspect, therapeutic combination contains about 2%-70%, 5%-60%, 10%- 50%, the active constituent of 15%-40%, 20%-30%, 25%-60%, 30%-60% or 35%-60%.

In one aspect, therapeutic combination can mix in tablet, immersion liquid, bolus, capsule or pre-composition.These are lived Property ingredient be configured to such dosage form and can be completed by method known to field of pharmaceutical preparations.See, e.g., United States Patent (USP) No.4,394,377.Capsule is easy to produce with the active constituent of any required form filling gelatine capsule.If desired, these materials Material can use inert powder to dilute dilution agent, such as sugar, starch, milk powder, the avicel cellulose etc. of purifying, with increase volume so as to In filling capsule.

In one aspect, conventional preparation method can be used for preparing the tablet containing therapeutic combination.In addition to the active ingredient (s, piece Agent can also contain alkali, disintegrating agent, absorbent, adhesive and lubricant.Typical alkali includes lactose, sugar, sodium chloride, starch and sweet Reveal alcohol.Starch and alginic acid are also good disintegrating agent.Sometimes also pungent using surfactant such as lauryl sodium sulfate and two Base sodium sulfosuccinate.Common absorbent includes starch and lactose.Magnesium carbonate is also applied for oily matter.For embodiment, What it is as adhesive is gelatin, natural gum, starch, dextrin, polyvinylpyrrolidone and various cellulose derivatives.Common lubrication Agent includes magnesium stearate, talcum, paraffin, various metallic soaps and polyethylene glycol.

In one aspect, in order to prepare the solid composite of such as tablet, by active constituent and pharmaceutical carrier (conventional pressure Piece ingredient, for example, cornstarch, lactose, sucrose, D-sorbite, talcum, stearic acid, magnesium stearate, Dicalcium Phosphate or natural gum or Other drugs diluent, such as water) mixing, to form the solid preformulation composition of the homogeneous mixture containing the present composition Object.When these pre-preparation compositions are known as uniform, it is intended that active constituent is evenly dispersed in entire composition, so that group Equivalent unit dosage forms, such as tablet, pill and capsule can be easily subdivided by closing object.Then by the solid preformulation group The unit dosage forms that object is subdivided into the above-mentioned type are closed, containing the desired amount of active constituent (for example, at least about 10⁵、10⁶、10⁷、 10⁸、10⁹、10¹⁰、10¹¹、10¹²Or 10¹³cfu).Therapeutic combination used herein can be seasoning.

In one aspect, therapeutic combination can be tablet or pill.It in an aspect, can be by tablet or pill packet Clothing is otherwise mixed to provide and have the dosage form for extending effect beneficial.For embodiment, tablet or pill may include interior Dosage and external dose component, the latter form coating on the former.Both components can be separated by enteric layer, and enteric layer is used for It resists the disintegration in stomach and internal composition is allowed completely to enter duodenum or sustained release.Multiple material can be used for this intestines Soluble layer or coating, this material include the material of many polymeric acids and polymeric acid and such as shellac, cetanol and cellulose acetate Mixture.

In one aspect, therapeutic combination is configured to delay or gradual enteric release form.In one aspect, delay or Gradual enteric release preparation includes using cellulose acetate, polyethylene glycol glycerol or both.In one aspect, delay or gradual Enteric release preparation includes using hydroxypropyl methyl cellulose (HPMC), microcrystalline cellulose (MCC), magnesium stearate or combinations thereof.? On one side, delay or gradual enteric release preparation include using poly- (methyl) acrylate, methacrylic acid copolymer B, first Base methyl acrylate, methacrylate, polyvinylpyrrolidone (PVP), PVP-K90 or combinations thereof.In one aspect, postpone Or gradual enteric release preparation includes the solid internal layer using folder between two outer layers；The solid internal layer includes the drug Composition and another component selected from disintegrating agent, burster, effervescent agent or any combination thereof；Wherein the outer layer includes basic Upper water-soluble, crystalline polymer or both.In one aspect, delay or gradual enteric release preparation include using not swellable Diffusion matrix.

In another aspect, delay or gradual enteric release preparation include using bilayer tablet or capsule, the bilayer Tablet or capsule include first layer again, and the first layer includes polyalkylene oxide, polyvinylpyrrolidone, lubricant or its mixing Object, and the second infiltration push layer includes the layer of polyethylene oxide, carboxymethyl cellulose or both.In one aspect, delay or Gradual enteric release preparation includes using hangover host material selected from the group below: acrylic polymer, cellulose, wax, Fatty acid, shellac, zeins, hydrogenated vegetable oil, rilanit special, polyvinylpyrrolidone, vinyl acetate copolymerization Object, ethenol copolymer, polyethylene oxide, acrylic acid and methacrylic acid copolymer, methylmethacrylate copolymer, methyl Ethoxyethyl acrylate polymer, amino alkyl methacrylate copolymer, gathers cynaoethyl methacrylate polymer (acrylic acid), poly- (methacrylic acid), methacrylic acid alkylamide copolymer, poly- (methyl methacrylate), poly- (methyl-prop Olefin(e) acid acid anhydride), methylmethacrylate polymer, polymethacrylates, poly- (methyl methacrylate) copolymer, polypropylene Amide, amino alkyl methacrylate copolymer, glycidyl methacrylate copolymer, methylcellulose, ethyl are fine Tie up element, carboxymethyl cellulose, hydroxypropyl methyl cellulose, hydroxymethyl cellulose, hydroxyethyl cellulose, hydroxypropyl cellulose, friendship Join sodium carboxymethylcellulose, cross-linked hydroxypropyl base cellulose, native paraffin, synthetic wax, fatty alcohol, fatty acid, aliphatic ester, fatty acid Glyceride, hydrogenated fat, chloroflo, stearic acid, stearyl alcohol, beeswax, sugared wax, castor wax, Brazil wax, polylactic acid, polyethanol Copolymer, carboxymethyl starch, the methacrylic acid potassium/divinyl benzene copolymer, crosslinked polyethylene pyrrole of acid, lactic acid and glycolic Pyrrolidone, polyalcohols alcohol, polyvinyl alcohol copolymer, polyethylene glycol, non-crosslinked polyvinylpyrrolidone, polyvinyl acetate, poly- second Vinyl acetate copolymer, or any combination thereof.In one aspect, delay or gradual enteric release preparation include using microenvironment pH Regulator.

In one aspect, therapeutic combination can be immersion liquid.In an aspect, controlling by selection salt water suspended form Composition is treated to prepare immersion liquid.A kind of water-soluble form of ingredient can make in conjunction with the water-insoluble form of another ingredient With by the suspension for preparing a kind of ingredient with the aqueous solution of another ingredient.Any active constituent of water-insoluble form Suspension can be prepared into or prepared in some physiologically acceptable solvents such as polyethylene glycol.Water-insoluble form is appointed A kind of suspension of active constituent can be in oil such as peanut, corn, sesame oil etc.；In ethylene glycol such as propylene glycol or polyethylene glycol In；Or it prepares in water, the solubility depending on given activity ingredient.In order to keep active constituent to suspend, it may be necessary to suitable Physiologically acceptable adjuvant.Adjuvant may include thickener, such as carboxymethyl cellulose, polyvinylpyrrolidone, gelatin And alginates.Surfactant, which is commonly used in suspended active ingredient, especially fat-soluble propionate, enhances compound.It is most useful in Suspension is prepared in liquid non-solvent is alkylphenol polyethylene oxide adduct, naphthalene sulfonate, alkylbenzene sulfonate and poly- Ethylene oxide sorbitan ester.In addition there are many substances, will affect the hydrophily, density and surface tension of liquid, have Help manufacture suspension on rare occasion.For embodiment, silicone antifoam agent, glycol, D-sorbite and sugar can be Suspending agent.

In one aspect, therapeutic combination include it is one or more, two or more, it is three or more or four kinds Or more clostridium species selected from the group below non-pathogenic spore: clostridium absonum, clostridium argentinense, clostridium Baratii, clostridium botulinum, clostridium cadaveris, clostridium carnis, clostridium celatum, clostridium chauvoei, clostridium Clostridioforme, clostridium cochlearium, clostridium fallax, clostridium felsineum, clostridium ghonii, clostridium Glycolicum, clostridium haemolyticum, clostridium hastiforme, clostridium histolyticum, clostridium indolis, clostridium Irregulare, clostridium limosum, clostridium malenominatum, clostridium novyi, clostridium oroticum, clostridium Paraputrificum, clostridium perfringens, clostridium piliforme, clostridium putrefaciens, clostridium Putrificum, clostridium sardiniense, clostridium sartagoforme, clostridium scindens, clostridium septicum, clostridium Sordellii, clostridium sphenoides, clostridium spiroforme, clostridium sporogenes, clostridium subterminale, clostridium Symbiosum, clostridium tertium, clostridium tetani, clostridium welchii and clostridium villosum.

In one aspect, therapeutic combination includes the non-pathogenic clostridium of purifying, separation or culture work and comes from Multiple purifying of one or more categories selected from the group below, separation or culture the non-pathogenic microorganism survived: Collins Salmonella, fecal bacteria, Dorea, Eubacterium and Ruminococcus.In another aspect, therapeutic combination includes to come from one or more A variety of purifying of a category selected from the group below, separation or culture non-pathogenic microorganisms: clostridium, Collins Salmonella, fecal bacteria, Dorea, Eubacterium and Ruminococcus.

In one aspect, therapeutic combination include two or more categories selected from the group below: Collins Salmonella, fecal bacteria, Dorea, Eubacterium and Ruminococcus.In another aspect, therapeutic combination includes two or more categories selected from the group below: Fecal bacteria, Dorea, Eubacterium and Ruminococcus.On the other hand, therapeutic combination include it is one or more, 2 kinds or more Kind, 3 kinds or more, 4 kinds or more or 5 kinds or more strains selected from the group below: fecal bacteria catus, fecal bacteria Comes, Dorea longicatena, Eubacterium eligens, Eubacterium hadrum, Eubacterium hallii, Eubacterium rectale With Ruminococcus torques.

In an aspect, therapeutic combination includes at least about 10⁵、10⁶、10⁷、10⁸、10⁹、10¹⁰、 10¹¹、10¹²Or 10¹³Or total cell count.In another aspect, therapeutic combination includes at most about 10⁵、10⁶、10⁷、10⁸、10⁹、10¹⁰、 10¹¹、10¹²、10¹³Or 10¹⁴Or total cell count.

In another aspect, therapeutic combination includes at least about 10⁵、10⁶、10⁷、10⁸、10⁹、 10¹⁰、10¹¹、10¹²Or 10¹³A cell or total cell count.In another aspect, therapeutic combination includes at most about 10⁵、10⁶、10⁷、10⁸、10⁹、 10¹⁰、10¹¹、10¹²、10¹³Or 10¹⁴A cell or total cell count.

In an aspect, pharmaceutical composition is in anaerobism packaging or container.In another aspect, pharmaceutical composition It also include oxygen scavenger.In an aspect, for embodiment, by being packed into oxygen removing machine that is built-in or clamping in a reservoir Structure (for example, deposited oxygen-scavenging particles as described in United States Patent (USP) No.7,541,091), can make container anaerobic.On the other hand In, container itself removes material (for example, oxygen removes iron or equivalent, such as O2BLOCK by oxygen^TMIt is described) it is made, Purifying and modified lamellar clay is used to remove the performance enhancement carrier of iron as oxygen；Active iron is directly dispersing in polymer In.In one embodiment, oxygen removes polymer and is used for manufacture container itself or coating container, or as to be added Grain；For example, describing as described in the U.S. Patent application of Publication No. 20110045222 with one or more ethylenic unsaturations Belong to the blend polymer of homopolymer or copolymer；One or more polyamide homopolymers or copolymer；Or one or more tools The polyethylene terephthalate homopolymer or copolymer of aerobic scavenging capacity.In one embodiment, oxygen removes polymerization Object is used for manufacture container itself or coating container, or as particle to be added；The U.S. such as Publication No. 20110008554 is special Described in benefit application, the composition comprising polyester, copolyester ether and oxidation catalyst is described, wherein copolyester ether includes containing poly- The polyether segment of (tetramethylene -co- alkylene ether).In one embodiment, oxygen scavenging polymer is used to prepare container sheet Body or coating container, or as particle to be added；For example, such as the U.S. Patent application institute of Publication No. 201000255231 It states, describes iron/salt particle of the dispersion in polymer substrate, and the oxygen with deposited oxygen-scavenging particles removes film.

A challenge for treating GI infection is the frequency height of recurrence or recurrence.Due to insufficient elimination infectant (for example, Pathogenic and/or alien bacteria), ongoing original symptom can be restored.Known bacterium does not divide sometimes and can be It survives in biomembrane in many wet (for example, internal) surfaces of body.Secondly, bacterium has spore, between sporogenesis Time of having a rest is more difficult to eradicate.Except non-sleep form is dividing, otherwise there is also the bacterium of suspend mode form, can be intracellular Extracellularly it is more difficult to the bacterium eradicated.Finally, Intracellular bacterial can be until the intestinal wall cell detachment where them to enteric cavity In, flora is infected again.In an alternate embodiment, the method for the present invention multiple or repeat intestinal flora infusion can with and can Shielded bacterium living can be needed to kill or otherwise inactivate in cell, biomembrane etc. (for example, infectious, pathogenic And/or exogenous).In an alternate embodiment, the method for the present invention multiple or repeat intestinal flora infusion can with and may Kill or otherwise inactivation of bacterial cell are needed, the bacterial cell is moved up along the crypts closer to chamber, at that In they fall in excrement stream and re-infect personal or patient.

In an aspect, pharmaceutical composition also includes biofilm disruption agent, or is used in combination with biofilm disruption agent.? In one aspect, biofilm disruption agent includes formalin.In an aspect, biofilm disruption agent includes one or more choosings From the enzyme of deoxyribonuclease (DNase), N-acetylcystein, alginate lyase and glycoside hydrolase dispersion element B.? In other side, biofilm disruption agent includes one or more components selected from the group below: quorum sensing inhibitor, ribonucleic acid It is III peptide for inhibiting, Salvadora persica extract, ability stimulator polypeptide, Patulin, penicillic acid, tubulin derived peptide, small Cleavage of peptide, PTP-7, nitric oxide, new emulsion, ozone, lytic phage, lactoferrin, xylitol hydrogel, synthesis iron chela Mixture, curcumin, Nano silver grain, acetyl -11- ketone-beta boswellic acid (AKBA), sinefungin, S-adenosylmethionine, S- adenosyl-homocysteine, Delisea furanone and N- sulfonyl homoserine lactone.In another aspect, biomembrane Disrupting agent includes bismuth-mercaptan compound (referring to WO2011/097347).

A method of gastrointestinal disorder that treating subject with this need, the method includes applying to the subject The pharmaceutical composition as described herein of pharmaceutical active dosage.In an aspect, gastrointestinal disorder being treated is inflammatory bowel Sick (IBD) or irritable bowel syndrome (IBS).In another aspect, the gastrointestinal disorder treated be selected from ulcerative colitis, gram Sieve grace disease, uncertain colitis, mucous colitis, collagenous colitis, chronic bacillary diarrhea (johne's disease), microscope colon Scorching, idiopathic inflammatory enteropathy and antibiotic-associated colitis.In an aspect, a kind of method further includes removing subject Attachment.

In an aspect, this application provides the method that IBD is treated in subject with this need, the method packets It includes to the subject and applies the first antibiotic or the probiotics of pharmaceutical active dosage to inhibit or antagonism Fusobacterium species.? In one aspect, repressed Fusobacterium species are selected from F.nucleatum, actinomyces pseudonecrophorus and F.varium.At another In aspect, the first probiotics includes pula clostridium species.In another aspect, the first probiotics includes pula clostridium.One In a aspect, a kind of method further includes applying one or more pula clostridium bacterium growth stimulants to subject.In another side In face, growth stimulant is selected from apple pectin, N-acetyl-glucosamine, cysteine, glutathione, riboflavin and flavine.Another On the one hand, a kind of method further includes the second antibiotic for applying pharmaceutical active dosage to the subject or the second probiotics to press down System or antagonism Mycobacterium species.In another aspect, repressed Mycobacterium species are perituberculosis mycobacteriums (MAP).In an aspect, the second probiotics include it is one or more, two or more, 3 kinds or more, 4 kinds or more Kind, 5 kinds or more, 6 kinds or more or 7 kinds or more anti-myco strains selected from the group below: corynebacteria, It is Dietzia, Gordonia, mycobacteria, Nocard's bacillus, beam village Salmonella, Skermania, butyric acid tomb village bacterium, Turicella, red Coccus and Williamsia.

In an aspect, the disclosure additionally provides the method treated in subject with this need or cure IBD, Wherein this method includes the pharmaceutical composition as described herein for removing the appendix of subject and applying pharmaceutical active dosage to subject Object.In another aspect, a kind of method further includes applying biofilm disruption agent, antibiotic or both to subject.At one In aspect, biofilm disruption agent and antibiotic can sequentially or simultaneously be applied by single composition.

In an aspect, had using composition as described herein or method to illness selected from the group below or obstacle is treated Effect: acne, AIDS enteropathy, the relevant gastroenteritis of AIDS, whole body alopecia, senile dementia, amyloidosis, amyotrophic side Rope sclerosis, ankylosing spondylitis, apositia, antibiotic-associated colitis, Asbergers syndrome, attention deficit barrier Hinder (ADD), attention deficit hyperactivity disorder (ADHD), autism spectrum disorder (ASD), Behcet syndrome, chronic difficult shuttle Bacterium infects (CDI), chronic constipation, chronic depression, chronic fatigue syndrome (CFS), the false obstructive synthesis of chronic idiopathic Sign, chronic inflammation Demyelinating Polyneuropathy, chronic nausea, chronic urticaria, celiaca, collagenous colitis, knot Intestinal polyp, the main FBD of constipation, Crohn disease, cryptogenic cirrhosis, cyclicity vomiting, dermatitis herpetiformis, diabetes, familial It is Mediterranean fruit fly, fatty liver, functional bowel disorder (FBD), gastroesophageal reflux, Gillian-Barre syndrome, glomerulonephritis, molten Hemorrhagic uremia syndrome, halitosis, based on IBS constipation, based on IBS diarrhea/constipation alternating, IBS diarrhea, based on IBS pain, it is special Hair property thrombocytopenic purpura (ITP), idiopathic/simple constipation, uncertain colitis, inflammatory bowel disease (IBD), intestines are easy Bowel syndrome (IBS), Lyme disease, manic-depressive psychosis, metabolic syndrome, microscopic colitis, migraine, mixes at adolescent diabetes Conjunction property cryoglobulinemia, mucous colitis, multiple sclerosis, myasthenia gravis, NASH (non-alcoholic fatty liver It is scorching), non-rheumatoid arthritis, non-rheumatoid factor positive arthritis, non-ulcer dyspepsia, Norwalk virus stomach and intestine Inflammation, obesity, obsessive-compulsive disorder, pain dominance FBD, Parkinson's disease, panarteritis, polyposis, primary biliary cirrhosis, original Hair property clostridium difficile infection (CDI), primary sclerotic cholangitis (PSC), pseudomembranous colitis, psychiatric diseases, Reiter syndrome, recurrent diverticulitis, Rett syndrome, rheumatoid arthritis, brandy nose, rotavirus gastroenteritis, sacrum Sacro-iliitis, schizophrenia, chorionitis, Sjogren syndrome, small bowel overgrowth, sudden infant death syndrome (SIDS), system Property lupus erythematosus, ulcerative colitis, upper abdomen FBD, vascular inflammatory disease, viral gastroenteritis, prediabetes syndrome, Type-1 diabetes mellitus, type-2 diabetes mellitus, depression, schizophrenia and emotional handicap.

Following exemplary embodiment is listed to be for illustration purposes only:

1. a kind of pharmaceutical composition, it is able to suppress or the micro- life of non-cause of disease of the work of antagonism Fusobacterium species it includes a variety of Object.

2. the pharmaceutical composition of embodiment 1, wherein the non-pathogenic microorganism of a variety of work is from synthesis culture.

3. the pharmaceutical composition of embodiment 1 or 2, wherein Fusobacterium species are selected from by actinomyces pseudonecrophorus, tool core shuttle bar Bacterium, F.canifelinum, F.gonidiaformans, fusobacterium mortiferum, F. naviforme, fusobacterium necrogenes, The group that F.russii, ulcer Fusobacterium and F.varium are formed.

4. the pharmaceutical composition of embodiment 1 or 2, wherein Fusobacterium species are selected from by F. nucleatum, downright bad shuttle The group of bacillus and F.varium composition.

5. the pharmaceutical composition of embodiment 1 or 2, wherein the non-pathogenic microorganism of a variety of work includes one or more Pula clostridium spp.

6. the pharmaceutical composition of embodiment 1 or 2, wherein the non-pathogenic microorganism of a variety of work includes pula clostridium.

7. the pharmaceutical composition of embodiment 1 or 2, wherein the non-pathogenic microorganism of a variety of work includes a kind of or more Kind, two or more, 3 kinds or more, 4 kinds or more, 5 kinds or more, 6 kinds or more or 7 kinds or more Or bacterial strain selected from the group below: pula clostridium prausnitzii A2-165, pula clostridium prausnitzii ATCC 27768, pula clostridium prausnitzii ATCC 27766, pula clostridium cF.prausnitzii KLE1255, pula clostridium Prausnitzii L2-6, pula clostridium prausnitzii M21/2, pula clostridium prausnitzii SL3/3, pula clostridium Sp.canine oral taxon 147, pula clostridium sp.DJF_VR20, pula clostridium sp.MC_41, pula clostridium sp.CAG: 1138, the pula pula clostridium sp.CAG:74, and clostridium sp. CAG:82.

8. the pharmaceutical composition of embodiment 1 or 2, wherein more than first non-pathogenic microorganism living includes to list in Fig. 1 Any pula clostridium bacterium.

9. the pharmaceutical composition of any one of embodiment 5 to 8, wherein described pharmaceutical composition also includes for pula shuttle The growth stimulant of bacterium bacterium.

10. the pharmaceutical composition of embodiment 9, wherein growth stimulant is selected from apple pectin, N-acetyl-glucosamine, half Guang Propylhomoserin, glutathione, riboflavin and flavine.

11. the pharmaceutical composition of any one of embodiment 1 to 10, wherein the composition is in anaerobism packaging or container In.

12. the pharmaceutical composition of any one of embodiment 1 to 11, wherein the composition also includes oxygen scavenger.

13. pharmaceutical composition, it includes be able to suppress or more than first non-cause of diseases living of antagonism Fusobacterium species are micro- It biology and is able to suppress or more than second non-pathogenic microorganisms living of antagonism Mycobacterium species.

14. the pharmaceutical composition of embodiment 13, wherein first, second or the non-pathogenic microorganism of two kind of a variety of work come from Synthesize culture.

15. the pharmaceutical composition of embodiment 13 or 14, wherein Fusobacterium species are selected from by actinomyces pseudonecrophorus, tool core shuttle Bacillus, F.canifelinum, F.gonidiaformans, fusobacterium mortiferum, F. naviforme, fusobacterium necrogenes, The group that F.russii, ulcer Fusobacterium and F.varium are formed.

16. the pharmaceutical composition of embodiment 13 or 14, wherein Fusobacterium species are selected from by F. nucleatum, necrosis The group of Fusobacterium and F.varium composition.

17. the pharmaceutical composition of any one of embodiment 13-16, wherein the Mycobacterium species are perituberculosis point Discrimination bacillus (MAP).

18. the pharmaceutical composition of any one of embodiment 13 to 17, wherein more than first non-pathogenic microorganism packet living Clostridium species containing pula.

19. the pharmaceutical composition of any one of embodiment 13 to 17, wherein more than first non-pathogenic microorganism packet living Include pula clostridium.

20. the pharmaceutical composition of any one of embodiment 13 to 17, wherein more than first non-pathogenic microorganism packet living Containing selected from by one or more of, two or more, 3 kinds or more, 4 kinds or more, 5 kinds or more, 6 kinds or More kinds of or 7 kinds or more isolates or bacterial strain: pula clostridium prausnitzii A2-165, pula clostridium Prausnitzii ATCC 27768, pula clostridium prausnitzii ATCC 27766, pula clostridium cF.prausnitzii KLE1255, pula clostridium prausnitzii L2-6, pula clostridium prausnitzii M21/2, pula clostridium Prausnitzii SL3/3, pula clostridium sp.canine oral taxon 147, pula clostridium sp.DJF_VR20, pula shuttle Bacterium sp.MC_41, pula clostridium sp.CAG:1138, the pula pula clostridium sp.CAG:74, and clostridium sp.CAG:82.

21. the pharmaceutical composition of any one of embodiment 13 to 17, wherein more than first non-pathogenic microorganism packet living Containing any pula clostridium bacterium listed in Fig. 1.

22. the pharmaceutical composition of any one of embodiment 13 to 21, wherein more than second non-pathogenic microorganism packet living Containing selected from by corynebacteria, Dietzia, Gordonia, mycobacteria, Nocard's bacillus, beam village Salmonella, Skermania, butyric acid tomb Village bacterium, Turicella, Rhodococcus sp and Williamsia composition anti-myco group it is one or more, two or more, 3 kinds or More kinds of, 4 kinds or more, 5 kinds or more, 6 kinds or more or 7 kinds or more.

23. the pharmaceutical composition of any one of embodiment 13 to 21, wherein more than second non-pathogenic microorganism packet living Containing selected from by Dietzia, Gordonia, mycobacteria, Nocard's bacillus and Rhodococcus sp form it is one or more, 2 kinds or more Kind, 3 kinds or more or 4 kinds or more.

24. the pharmaceutical composition of any one of embodiment 13 to 21, wherein more than second non-pathogenic microorganism packet living Containing Dietzia.

25. the pharmaceutical composition of any one of embodiment 13 to 21, wherein more than second non-pathogenic microorganism packet living Containing selected from by D.aerolata, D.alimentaria, D.aurantiaca, D. cerdiciphylli, D.cinnamea, D.kunjamensis、D.lutea、D.maris、D. natronolimnaea、D.papillomatosis、 D.psychralcaliphila, D.schimae and D. timorensis composition it is one or more, two or more, 3 kinds Or more, 4 kinds or more, 5 kinds or more, 6 kinds or more or 7 kinds or more.

26. the pharmaceutical composition of any one of embodiment 13 to 21, wherein more than second non-pathogenic microorganism packet living Containing selected from by G.aichiensis, G.alkanivorans, G.amarae, G.amicalis, G.araii, G.bronchialis、G.defluvii、G.desulfuricans、G.effusa、G.hirstuta、 G.hydrophobica、 G.lacunae、G.malaquae、G.namibiensis、G.otitidis、G. paraffinivorans、 G.polyisoprenivorans、G.rhizosphera、G.rubripertincta、G. shandongensis、 G.sihwensis, G.sinesedis, G.soli, G.sputi, G.terrae, and G. westfalica composition one kind or It is a variety of, two or more, 3 kinds or more, 4 kinds or more, 5 kinds or more, 6 kinds or more or 7 kinds or more Kind.

27. the pharmaceutical composition as described in any one of embodiment 13 to 21, wherein more than described second non-disease living Pathogenic microorganism include selected from by C.accolens, C.afermentans ssp. afermentans, C.ammoniagenes, C.amycolatum、C.appendicis、C.aquilae、 C.argentoratense、C.atypicum、 C.aurimucosum、C.auris、C.auriscanis、 C.bovis、C.callunae、C.camporealensis、 C.canis、C.capitovis、C.casei、 C.caspium、C.ciconiae、C.confusum、C.coyleae、 C.cystitidis、C.diphtheria、 C.doosanense、C.durum、C.efficiens、C.falsenii、 C.felinum、C.flavescens、 C.freiburgense、C.freneyi、C.glaucum、 C.glucuronolyticum、C.glutamicum、 C.halotolerans、C.hansenii、C.imitans、 C.jeikeium、C.kroppenstedtii、C. kutscheri、C.lipophiloflavum、C.lubricantis、 C.macginleyi、C.marinum、 C.maris、C.massiliense、C.mastitidis、C.matruchotii、 C.minutissimum、 C.mucifaciens、C.mustelae、C.mycetoides、C.phocae、C.pilbarense、 C. pilosum、C.propinquum、C.pseudodiphtheriticum、C.pseudotuberculosis、 C.pyruviciproducens、C.renale、C.resistens、C.riegelii、C.simulans、C. singular、 C.sphenisci、C.spheniscorum、C.sputi、C.stationis、C.striatum、 C.suicordis、 C.sundsvallense、C.terpenotabidum、C.testudinoris、C. thomssenii、C.timonense、 C.tuberculostearicum、C.tuscaniense、C.ulcerans、 C.ulceribovis、C.urealyticum、 C.ureicelerivorans, C.variabile, C. vitaeruminis and C.xerosis composition it is one or more, 2 kinds Or more, 3 kinds or more, 4 kinds or more, 5 kinds or more, 6 kinds or more or 7 kinds or more rod-like stems Bacterium.

28. the pharmaceutical composition of any one of embodiment 13 to 21, wherein more than second non-pathogenic microorganism packet living Containing selected from by mycobacterium tuberculosis, M.leprae, M.avium-intracellulare, M.bovis, M.cheloiei, M.africanum、M.marinium、M.buruli、M.fortuitum、 M.haemophilum、M.intracellulare、 M.kansasii、M.littorale、M.malmoense、 M.marianum、M.sinuae、M.szulgai、and M.ulcerans, the one or more of M.avium, M. flavascens, M.lepraemurium and M.nicroti composition, 2 Kind or more, 3 kinds or more, 4 kinds or more, 5 kinds or more, 6 kinds or more or 7 kinds or more branches Bacillus species.

29. the pharmaceutical composition of any one of embodiment 13 to 21, wherein more than second non-pathogenic microorganism packet living Containing selected from by N.abscessus, N.acidivorans, N.africana, N.alba, N.altamirensis, N.amamiensis、N.anaemiae、N.aobensis、N.araoensis、 N.arthritidis、N.asiatica、 N.asteroides、N.beijingensis、N.blacklockiae、 N.brasiliensis、N.brevicatena、 N.caishijiensis、N.calitrisensis、N.carnea、 N.cerradoensis、N.concava、 N.coubleae、N.crassostreae、N.cummidelens、 N.cyriacigeorgica、N.elegans、 N.exalbida、N.farcinica、N.flavorosea、 N.fluminea、N.gamkensis、N.harensis、 N.higoensis、N.ignorata、N. inohanensis、N.iowensis、N.jejuensis、N.jiangxiensis、 N.jinanensis、N. kruczakiae、N.lijiangensis、N.mexicana、N.miyunensis、 N.neocaledoniensis、 N.niigataensis、N.ninae、N.nova、N.otitidiscaviarum、 N.paucivorans、 N.pigrifrangens、N.pneumoniae、N.polyresistens、 N.pseudobrasiliensis、 N.pseudovaccinii、N.puris、N.salmonicida、N.seriolae、 N.shimofusensis、 N.sienata、N.soli、N.speluncae、N.takedensis、N.tenerifensis、 N.terpenica、 N.testacea、N.thailandica、N.transvalensis、N.uniformis、N.vaccinii、 N. vermiculata, N.veterana, N.vinacea, N.wallacei, N.xishanensis and N. Yamanashiensis composition it is one or more, two or more, 3 kinds or more, 4 kinds or more, 5 kinds or more Kind, 6 kinds or more or 7 kinds or more Nocard's bacillus.

30. the pharmaceutical composition of any one of embodiment 13 to 21, wherein more than second non-pathogenic microorganism packet living Containing selected from by R.aurantiacus, R.aetherivorans, R.baikonurensis, R. coprophilus, R.corynebacterioides、R.equi、R.erythropolis、R.fascians、 R.globerulus、 R.gordoniae、R.imtechensis、R.jostii、R.koreensis、R. kroppenstedtii、 R.kunmingensis、R.kyotonensis、R.maanshanensis、R. marinonascens、R.opacus、 R.percolatus、R.phenolicus、R.pyridinivorans、 R.qingshengii、R.rhodnii、 R.rhodochrous、R.ruber、R.triatomae、R. tukisamuensis、R.wratislaviensis、 R.yunnanensis and R.zopfii composition it is one or more, two or more, 3 kinds or more, 4 kinds or more, 5 Kind or more, 6 kinds or more or 7 kinds or more Rhodococcus sp strains.

31. the pharmaceutical composition of any one of embodiment 13 to 21, wherein more than second non-pathogenic microorganism packet living Containing selected from by Skermania piniformis, Williamsia deligens, Williamsia serinedens, Williamsia maris、Williamsia marianensis、Williamsia muralis、 and Williamsia Faeni composition it is one or more, two or more, 3 kinds or more, 4 kinds or more, 5 kinds or more, 6 kinds or It is more kinds of or 7 kinds.

32. the pharmaceutical composition of any one of embodiment 13 to 21, wherein more than second non-pathogenic microorganism packet living Containing selected from by T.paurometabola, T.spumae, T.inchonensis, T. sunchonensis, T.pseudospumae, T.spongiae, T.pulmonis, T.tyrosinosolvens, and T.strandjordii group At it is one or more, two or more, 3 kinds or more, 4 kinds or more, 5 kinds or more, 6 kinds or more or 7 kinds or more butyric acid tombs village bacterium strain.

33. the pharmaceutical composition of any one of embodiment 13 to 32, wherein more than first non-pathogenic microorganism living, the The combined pharmacologically active agents of more than two non-pathogenic microorganism living or more than first and second non-pathogenic microorganisms living Amount is selected from the group being made of following dosage: 10³cfu-10¹⁴cfu、10⁴cfu-10¹⁴cfu、10⁵cfu-10¹⁴cfu、10⁶cfu- 10¹⁴cfu、10⁷cfu-10¹⁴cfu、 10⁸cfu-10¹⁴cfu、10⁴cfu-10¹³cfu、10⁵cfu-10¹²cfu、10⁶cfu- 10¹¹cfu、10⁷cfu-10¹⁰cfu、 10⁸cfu-10⁹cfu、10³cfu-10¹³cfu、10³cfu-10¹²cfu、10³cfu- 10¹¹cfu、10³cfu-10¹⁰cfu、10³cfu-10⁹cfu、10³cfu-10⁸cfu、10³cfu-10⁷cfu、10³cfu-10⁶cfu、 10³cfu-10⁵cfu、 10³cfu-10⁴cfu。

34. the pharmaceutical composition of any one of embodiment 13 to 32, wherein more than first non-pathogenic microorganism living, the The combined pharmacologically active agents of more than two non-pathogenic microorganism living or more than first and second non-pathogenic microorganisms living Amount is selected from the group being made of following dosage: 10⁸cfu-10¹⁴cfu、 10⁹cfu-10¹³cfu、10¹⁰cfu-10¹²cfu、10⁹cfu- 10¹⁴cfu、10⁹cfu-10¹²cfu、 10⁹cfu-10¹¹cfu、10⁹cfu-10¹⁰cfu、10¹⁰cfu-10¹⁴cfu、10¹⁰cfu- 10¹³cfu、 10¹¹cfu-10¹⁴cfu、10¹¹cfu-10¹³cfu、10¹²cfu-10¹⁴cfu、10¹³cfu-10¹⁴cfu。

35. the pharmaceutical composition of any one of embodiment 13 to 32, wherein more than first non-pathogenic microorganism living, the The combined pharmacologically active agents of more than two non-pathogenic microorganism living or more than first and second non-pathogenic microorganisms living Amount includes up to: 10³、10⁴、10⁵、10⁶、10⁷、10⁸、10⁹、10¹⁰、10¹¹、10¹²、10¹³、10¹⁴、10¹⁵cfu。

36. the pharmaceutical composition of any one of embodiment 13 to 32, wherein more than first non-pathogenic microorganism living, the The combined pharmacologically active agents of more than two non-pathogenic microorganism living or more than first and second non-pathogenic microorganisms living Amount includes up to: 10³、10⁴、10⁵、10⁶、10⁷、10⁸、 10⁹、10¹⁰、10¹¹、10¹²、10¹³、10¹⁴、10¹⁵cfu。

37. the pharmaceutical composition of any one of embodiment 13 to 32, wherein more than first non-pathogenic microorganism living, the The combined pharmacologically active agents of more than two non-pathogenic microorganism living or more than first and second non-pathogenic microorganisms living Amount is comprising selected from by 10³-10¹⁴、10⁴-10¹⁴、10⁵-10¹⁴、 10⁶-10¹⁴、10⁷-10¹⁴、10⁸-10¹⁴、10⁴-10¹³、10⁵-10¹²、 10⁶-10¹¹、10⁷-10¹⁰、10⁸-10⁹、 10³-10¹³、10³-10¹²、10³-10¹¹、10³-10¹⁰、10³-10⁹、10³-10⁸、10³- 10⁷、10³-10⁶、 10³-10⁵、10³-10⁴The cell count of composition.

38. the pharmaceutical composition of any one of embodiment 13 to 32, wherein more than first non-pathogenic microorganism living, the The combined pharmacologically active agents of more than two non-pathogenic microorganism living or more than first and second non-pathogenic microorganisms living Amount is comprising selected from by 10⁸-10¹⁴、10⁹-10¹³、10¹⁰-10¹²、 10⁹-10¹⁴、10⁹-10¹²、10⁹-10¹¹、10⁹-10¹⁰、10¹⁰- 10¹⁴、10¹⁰-10¹³、10¹¹-10¹⁴、10¹¹-10¹³、 10¹²-10¹⁴、10¹³-10¹⁴The cell count of composition.

39. the pharmaceutical composition of any one of embodiment 13 to 32, wherein more than first non-pathogenic microorganism living, the The combined pharmacologically active agents of more than two non-pathogenic microorganism living or more than first and second non-pathogenic microorganisms living Amount includes at most 10³、10⁴、10⁵、10⁶、10⁷、10⁸、 10⁹、10¹⁰、10¹¹、10¹²、10¹³、10¹⁴、10¹⁵Cell count.

40. the pharmaceutical composition of any one of embodiment 13 to 32, wherein more than first non-pathogenic microorganism living, the The combined pharmacologically active agents of more than two non-pathogenic microorganism living or more than first and second non-pathogenic microorganisms living Amount includes at most 10³、10⁴、10⁵、10⁶、10⁷、10⁸、 10⁹、10¹⁰、10¹¹、10¹²、10¹³、10¹⁴、10¹Cell count.

41. the pharmaceutical composition of any one of embodiment 13 to 40, wherein described pharmaceutical composition be liquid, freezing, Freeze-drying, spray drying, freeze-drying or powder type.

42. the pharmaceutical composition of any one of embodiment 13 to 41, wherein described pharmaceutical composition includes excipient, salt Water, buffer, buffer or fluid-glucose-cellobiose agar (RGCA) culture medium.

43. the pharmaceutical composition of any one of embodiment 13 to 42, wherein described pharmaceutical composition is configured to enteric Clothing capsule or microcapsules, acidproof capsule or microcapsules, acidproof tablet, are suitable for recovery, nose duodenum infusion at enteric coated tablet Or the powder delivered in the form of bowel lavage or colon perfusion.

44. the pharmaceutical composition of any one of embodiment 13 to 42, wherein described pharmaceutical composition is configured to postpone Or gradual enteric release form.

45. the pharmaceutical composition of embodiment 44, wherein delay or gradual enteric release preparation include using acetate fiber Element, polyethylene glycol glycerol or both.

46. the pharmaceutical composition of embodiment 44, wherein delay or gradual enteric release preparation include using hydroxypropyl first Base cellulose (HPMC), microcrystalline cellulose (MCC), magnesium stearate or combinations thereof.

47. the pharmaceutical composition of embodiment 44, wherein delay or gradual enteric release preparation include using poly- (methyl) Acrylate, methacrylic acid copolymer B, methyl methacrylate, methacrylate, polyvinylpyrrolidone (PVP), PVP-K90 or combinations thereof.

48. the pharmaceutical composition of embodiment 44, wherein delay or gradual enteric release preparation include that use is clipped in two Solid internal layer between outer layer；Wherein solid internal layer includes that pharmaceutical composition and another kind are selected from disintegrating agent, burster, effervescent agent Or any combination thereof component；Wherein outer layer includes substantially water-soluble, crystalline polymer or both.

49. the pharmaceutical composition of embodiment 44, wherein delay or gradual enteric release preparation include using not swellable Diffusion matrix.

50. the pharmaceutical composition of embodiment 44, wherein delay or gradual enteric release preparation include using bilayer tablet Or capsule, it includes the first layer containing or mixtures thereof polyalkylene oxide, polyvinylpyrrolidone, lubricant and include polycyclic oxygen Second infiltration push layer of ethane, carboxymethyl cellulose or both.

51. the pharmaceutical composition of embodiment 44, wherein delay or gradual enteric release preparation include using selected under The hangover host material of group composition: acrylic polymer, cellulose, wax, fatty acid, shellac, zeins, hydrogen Change vegetable oil, rilanit special, polyvinylpyrrolidone, vinyl acetate copolymer, ethenol copolymer, polyethylene oxide, Acrylic acid and methacrylic acid copolymer, methylmethacrylate copolymer, ethoxyethyl methacrylates polymer, methyl Acrylic acid cyanogen polymerizable methacrylate object, amino alkyl methacrylate copolymer, poly- (acrylic acid), poly- (methacrylic acid), methyl Acrylic acid alkyl amide copolymer, poly- (methyl methacrylate), poly- (methacrylic anhydride), methyl methacrylate polymerization Object, polymethacrylates, poly- (methyl methacrylate) copolymer, polyacrylamide, amino alkyl methacrylate are total Polymers, glycidyl methacrylate copolymer, methylcellulose, ethyl cellulose, carboxymethyl cellulose, hydroxypropyl methyl Cellulose, hydroxymethyl cellulose, hydroxyethyl cellulose, hydroxypropyl cellulose, croscarmellose sodium, cross-linked hydroxypropyl base are fine Tie up element, native paraffin, synthetic wax, fatty alcohol, fatty acid, aliphatic ester, fatty glyceride, hydrogenated fat, chloroflo, stearic acid, Stearyl alcohol, beeswax, sugared wax, castor wax, Brazil wax, polylactic acid, polyglycolic acid, copolymer lactic acid and glycolic, carboxymethyl Starch, methacrylic acid potassium/divinyl benzene copolymer, crosslinked polyvinylpyrrolidone, poly- alkanol, polyvinyl alcohol copolymer, Polyethylene glycol, non-crosslinked polyvinylpyrrolidone, polyvinyl acetate, polyvinyl acetate copolymer or their any group It closes.

52. the pharmaceutical composition of embodiment 44, wherein delay or gradual enteric release preparation include using microenvironment pH Regulator.

53. the pharmaceutical composition as described in any one of embodiment 13 to 42, wherein the composition and food, liquid Beverage, food additives, milk-based products, product based on soybean or derivatives thereof, jelly or Yoghourt are applied together.

54. the pharmaceutical composition as described in any one of embodiment 13 to 53, wherein more than described first non-disease living The non-pathogenic microorganism of pathogenic microorganism, the non-pathogenic microorganism of more than second work or more than first and second work Combination is in anaerobism packaging or container.

55. the pharmaceutical composition as described in any one of embodiment 13 to 53, wherein more than described first non-disease living The non-pathogenic microorganism of pathogenic microorganism, the non-pathogenic microorganism of more than second work or more than first and second work Combination is in aerobic packaging or container.

56. the pharmaceutical composition of any one of embodiment 1 to 55, wherein described pharmaceutical composition includes cryoprotection Agent.

57. the pharmaceutical composition of embodiment 56, wherein the cryoprotector includes polyethylene glycol, skimmed milk, red moss Sugar alcohol, arabite, D-sorbite, glucose, fructose, alanine, glycine, proline, sucrose, lactose, ribose, seaweed Sugar, dimethyl sulfoxide (DMSO), glycerol or combinations thereof.

58. the pharmaceutical composition as described in any one of embodiment 1 to 57, wherein described pharmaceutical composition also includes acid Inhibitor, antiacid, H₂Antagonist, proton pump inhibitor or combinations thereof.

59. the pharmaceutical composition of any one of embodiment 1 to 58, wherein described pharmaceutical composition also includes the micro- life of excrement Object preparation.

60. a kind of pharmaceutical composition, it includes the fecal microorganism group from single donor subject, application has one kind Or a variety of pula clostridium species or one or more growth stimulants at least one pula clostridium species, wherein relative to Control fecal microorganism from the identical donor subject for not applying one or more growth stimulants, the fecal microorganism Include raised levels of at least one pula clostridium species.

61. the pharmaceutical composition of embodiment 60, wherein donor subject absorb one or more pula clostridium species or One or more growth stimulants.

62. the pharmaceutical composition of embodiment 60 or 61, wherein one or more growth stimulants are selected from Apples The group of glue, N-acetyl-glucosamine, cysteine, glutathione, riboflavin and flavine composition.

63. the pharmaceutical composition as described in any one of embodiment 60 to 62 is applied wherein the fecal microorganism comes from With at least about 1 after growth stimulant, 2,3,4,5,6,7,8,9,10,11,12,13,14,18,20,24,28,30 or 36 hours The fecal specimens of collection.

64. the pharmaceutical composition of any one of embodiment 60 to 62 is given birth to wherein the fecal microorganism comes from application At least about 1 after long stimulant, 2,3,4,5 or 6 days collect fecal specimens.

65. the pharmaceutical composition as described in any one of embodiment 60 to 62, wherein by one or more growths Stimulant was applied to the donor subject more than about 1,2,3,4,5,6,7,8,9,10,11,12,13 or 14 days.

66. the pharmaceutical composition as described in any one of embodiment 60 to 62, wherein by one or more growths Stimulant was applied to the donor subject more than about 1,2,3,4,5,6,7,8,9,10,11,12,13 or 14 weeks.

67. the pharmaceutical composition as described in any one of embodiment 60 to 66, wherein by one or more growths Stimulant is applied to donor subject at least 1,2,3,4,5,6,7,8,9 or 10 time daily.

68. a kind of pharmaceutical composition, it includes non-synthetic fecal microorganisms, wherein the non-synthetic fecal microorganism is opposite Include raised levels of at least one pula clostridium species in the control fecal microorganism from normal healthy donors.

69. a kind of pharmaceutical composition, it includes non-selected fecal microorganisms, wherein the non-selected fecal microorganism The fecal microorganism non-selected relative to the control from normal healthy donors includes raised levels of at least one pula clostridium Strain.

70. a kind of pharmaceutical composition, it includes the untreated non-synthetic fecal microorganism from single donor subject, Wherein the untreated non-synthetic fecal microorganism includes to rise relative to the control fecal microorganism from normal healthy donors High-caliber at least one pula clostridium species.

71. the pharmaceutical composition of any one of embodiment 60 to 70, wherein elevated levels are selected from 1.5 times or more Again, 2 times or more, 2.5 times or more, 3 times or more, 3.5 times or more, 4 times or more, 5 times or more, 10 times or more, 50 times or more, 100 times or more, 1000 times or more and 10,000 times or more.

72. the pharmaceutical composition as described in any one of embodiment 60 to 70, wherein the elevated levels be selected from by with The group of lower composition: at least 10% or more, at least 15% or more, at least 20% or more, at least 25% or more, at least 30% or more, At least 40% or more, at least 50% or more, at least 60% or more, at least 70% or more, at least 80% or more, at least 90% with It is upper, at least 100% or more, at least 150% or more, at least 200% or more, at least 250% or more, at least 300% or more, at least 350% or more, at least 400% or more, at least 450% or more, at least 500% or more, at least 600% or more, at least 700% Above, at least 800% or more.

73. the pharmaceutical composition of any one of embodiment 59 to 72, wherein the fecal microorganism or fecal microorganism Preparation includes the complete or essentially completed microorganism of donor.

74. the pharmaceutical composition of any one of embodiment 59 to 72, wherein the fecal microorganism or fecal microorganism Preparation includes non-selected fecal microorganism.

75. the pharmaceutical composition of any one of embodiment 59 to 72, wherein the fecal microorganism or fecal microorganism Preparation includes separation or purifying work non-pathogenic fecal bacteria group.

76. the pharmaceutical composition of any one of embodiment 59 to 72, wherein fecal microorganism or fecal microorganism preparation Preparation be related to selected from alcohol treatment, detergent-treatment, heat treatment, radiation and the processing of ultrasonic treatment or their combination.

77. the pharmaceutical composition of any one of embodiment 59 to 72, wherein fecal microorganism or fecal microorganism preparation Preparation be not related to selected from alcohol treatment, detergent-treatment, heat treatment, radiation and ultrasonic treatment processing.

78. the pharmaceutical composition of any one of embodiment 59 to 72, the wherein preparation of fecal microorganism or preparation include Separating step selected from filtering, screening, density gradient, filtering, chromatography and combinations thereof.

79. the pharmaceutical composition of any one of embodiment 59 to 72, wherein the fecal microorganism or fecal microorganism Preparation is not needed selected from filtering, screening, density gradient, filtering and chromatographic one or more separating steps.

80. the pharmaceutical composition of any one of embodiment 59 to 72, wherein fecal microorganism or fecal microorganism preparation Substantially free of abitotic substance.

81. the pharmaceutical composition of any one of embodiment 59 to 72, wherein fecal microorganism or fecal microorganism preparation Substantially free of the cell-free material for being selected from remnant fibrous, DNA, viral coat material and non-viable bacteria material.

82. the pharmaceutical composition of any one of embodiment 59 to 72, wherein fecal microorganism or fecal microorganism preparation Substantially free of the eukaryocyte from fecal microorganism group's donor.

83. the pharmaceutical composition of embodiment 59, wherein the fecal microorganism preparation carrys out the fecal materials of via Self-reconfiguration.

84. the pharmaceutical composition of embodiment 59, wherein the fecal microorganism preparation is from synthesis fecal materials.

85. the pharmaceutical composition of any one of embodiment 59 to 72, wherein the fecal microorganism or fecal microorganism Preparation does not include antibiotic resistance group.

86. the pharmaceutical composition of embodiment 59, wherein the fecal microorganism preparation includes the living flora of proportional amount Preparation is similar to normal healthy people faecal microbiota.

87. the pharmaceutical composition of any one of embodiment 59 to 72, wherein fecal microorganism group or the micro- life of excrement Object group's preparation includes the bacterium from least 2,3,4,5,6,7,8,9,10,12,15,18 or 20 different families.

88. the pharmaceutical composition of any one of embodiment 59 to 72, wherein the fecal microorganism or fecal microorganism Preparation includes to come from least 2,3,4,5,6,7,8,9,10,12,15,18,20,23,25,27,30,32,35,38 or 40 not The bacterium belonged to.

89. the pharmaceutical composition of any one of embodiment 59 to 72, wherein the fecal microorganism or fecal microorganism Preparation has the Shannon diversity index of 0.4-5.0 in family, category or species level.

90. the pharmaceutical composition of any one of embodiment 59 to 72, wherein the fecal microorganism or fecal microorganism Preparation has at least about 20%, 30%, 40%, 50%, 60%, 70%, 80%, 85%, 90%, 95%, 99% or 99.5% Spore form microorganism.

91. the pharmaceutical composition as described in any one of embodiment 59 to 72, wherein the fecal microorganism or excrement Microorganism formulation have at least about 20%, 30%, 40%, 50%, 60%, 70%, 80%, 85%, 90%, 95%, 99% or The microorganism of 99.5% non-spore form.

92. the pharmaceutical composition as described in any one of embodiment 59 to 72, wherein the fecal microorganism or excrement Microorganism formulation by it is one or more, two or more, 3 kinds or more, 4 kinds or more or 5 kinds or more trainings Feeding fecal microorganism is further supplemented or enhances.

93. the pharmaceutical composition of embodiment 92, wherein it is described it is one or more, one or more, 2 kinds or more, 3 kinds or more, 4 kinds or more or 5 kinds or more fecal microorganisms are spore form.

94. the pharmaceutical composition of embodiment 92, wherein it is described it is one or more, two or more, 3 kinds or more Kind, 4 kinds or more or 5 kinds or more fecal microorganisms are selected from the group: amino acid coccus, Ackermam bacterium, Alistipes, Anaerotruncus, Bacteroides, Bifidobacterium, Blaw spy Salmonella, Butyrivibrio, clostridium, Collins Salmonella, excrement ball Bacterium, corynebacteria, Dorea, enterococcus, Escherichia, Eubacterium, pula clostridium, haemophilus, Holdemania, lactic acid bacteria, Catarrhalis, Parabacteroides, Prey irrigate bacterium, Propionibacterium, Raoul bacterium, caecum Ross Salmonella, Ruminococcus, Portugal Grape coccus, streptococcus, rare micrococcus and Veillonella.

95. the pharmaceutical composition of embodiment 92, wherein it is described it is one or more, two or more, 3 kinds or more Kind, 4 kinds or more or 5 kinds or more fecal microorganisms are selected from: Bacteroides fragilis ssp.vulgatus, Collins Salmonella aerofaciens, Bacteroides fragilis ssp. thetaiotaomicron, Pepto streptococcus Productus II, Parabacteroides distasonis, pula clostridium prausnitzii, fecal bacteria eutactus, Pepto streptococcus productus, Ruminococcus bromii, Bifidobacterium adolescentis, Gemmiger Formicilis, Bifidobacterium longum, Eubacterium siraeum, Ruminococcus torques, Eubacterium rectale, Eubacterium Eligens, Bacteroides eggerthii, clostridium leptum, Bacteroides fragilis ssp.A, Eubacterium Biforme, Bifidobacterium infantis, Eubacterium rectale, fecal bacteria comes, Pseudoflavonifractor Capillosus, Ruminococcus albus, Dorea formicigenerans, Eubacterium hallii, Eubacterium ventriosum, Russian Fusobacterium, Ruminococcus obeum, Eubacterium rectale, clostridium ramosum, lactic acid bacteria leichmannii, cud ball Bacterium callidus, Butyrivibrio crossotus, amino acid coccus fermentans, Eubacterium ventriosum, Bacteroides fragilis ssp.fragilis, fecal bacteria catus, Aerostipes hadrus, Eubacterium Cylindroides, Eubacterium ruminantium, staphylococcus epidermidis, Eubacterium limosum, Tissirella Praeacuta, Fusobacterium mortiferum, Fusobacterium naviforme, clostridium innocuum, clostridium Ramosum, Propionibacterium acnes, Ruminococcus flavefaciens, Bacteroides fragilis ssp.ovatus, Fusobacterium nucleatum, Fusobacterium mortiferum, Escherichia coli, Gemella Morbillorum, Finegoldia magnus, streptococcus intermedius, Ruminococcus lactaris, Eubacterium tenue, Eubacterium ramulus, Bacteroides clostridiiformis ssp.clostridliformis, Bacteroides Coagulans, Prey irrigate bacterium oralis, Prey irrigate bacterium ruminicola, Odoribacter splanchnicus and Desuifomonas pigra。

96. the pharmaceutical composition of any one of embodiment 59 to 72, wherein fecal microorganism or fecal microorganism preparation Lack at least one, at least two kinds of, at least three kinds of or at least four kinds of bacterium categories selected from the group below: amino acid coccus, Ackermam bacterium, Alistipes, Anaerotruncus, Bacteroides, Bifidobacterium, Blaw spy Salmonella, Butyrivibrio, clostridium, Ke Lin This Salmonella, fecal bacteria, corynebacteria, Dorea, enterococcus, Escherichia, Eubacterium, haemophilus, Holdemania, lactic acid Bacterium, catarrhalis, Parabacteroides, Prey irrigate bacterium, Propionibacterium, Raoul bacterium, caecum Ross Salmonella, Ruminococcus, Staphylococcus, streptococcus, rare micrococcus and Veillonella.

97. the pharmaceutical composition of any one of embodiment 59 to 72, wherein fecal microorganism or fecal microorganism preparation Lack at least one, at least two kinds of, at least three kinds of or at least 4 kinds of microorganisms selected from the group below: Bacteroides fragilis Ssp.vulgatus, Collins Salmonella aerofaciens, Bacteroides fragilis Ssp.thetaiotaomicron, Pepto streptococcus productus II, Parabacteroides distasonis, pula Clostridium prausnitzii, fecal bacteria eutactus, Pepto streptococcus productus, Ruminococcus bromii, Bifidobacterium Adolescentis, Gemmiger formicilis, Bifidobacterium longum, Eubacterium siraeum, Ruminococcus Torques, Eubacterium rectale, Eubacterium eligens, Bacteroides eggerthii, clostridium leptum, Bacteroides fragilis ssp.A, Eubacterium biforme, Bifidobacterium infantis, Eubacterium rectale, excrement ball Bacterium comes, Pseudoflavonifractor capillosus, Ruminococcus albus, Dorea formicigenerans, Eubacterium hallii, Eubacterium ventriosum, Russian Fusobacterium, Ruminococcus obeum, Eubacterium rectale, clostridium Ramosum, lactic acid bacteria leichmannii, Ruminococcus callidus, Butyrivibrio crossotus, amino acid coccus Fermentans, Eubacterium ventriosum, Bacteroides fragilis ssp.fragilis, fecal bacteria catus, Aerostipes hadrus, Eubacterium cylindroides, Eubacterium ruminantium, staphylococcus epidermidis, Eubacterium limosum, Tissirella praeacuta, Fusobacterium mortiferum, Fusobacterium Naviforme, clostridium innocuum, clostridium ramosum, Propionibacterium acnes, Ruminococcus flavefaciens, Bacteroides fragilis ssp.ovatus、Fusobacterium nucleatum、 Fusobacterium Mortiferum, Escherichia coli, Gemella morbillorum, Finegoldia magnus, streptococcus Intermedius, Ruminococcus lactaris, Eubacterium tenue, Eubacterium ramulus, Bacteroides Clostridiiformis ssp.clostridliformis, Bacteroides coagulans, Prey irrigate bacterium oralis, general Thunder irrigates bacterium ruminicola, Odoribacter splanchnicus and Desuifomonas pigra.

98. the pharmaceutical composition of any one of foregoing embodiments, wherein described pharmaceutical composition is also broken comprising biomembrane Bad agent.

99. the pharmaceutical composition of embodiment 98, wherein the biofilm disruption agent includes one or more selected from deoxidation Ribalgilase (DNase), N-acetylcystein, alginate lyase and glycoside hydrolase disperse the enzyme of element B.

100. the pharmaceutical composition of embodiment 98, wherein the biofilm disruption agent includes selected from the group below a kind of or more Kind component: quorum sensing inhibitor, ribonucleic acid III peptide for inhibiting, Salvador extract, ability stimulator polypeptide, patulin, blueness Mould acid, tubulin derived peptide, small cleavage of peptide, PTP-7, nitric oxide, new emulsion, ozone, lytic phage, lactoferrin, Xylitol hydrogel, synthesis iron chelating agent, curcumin, Nano silver grain, acetyl group -11- ketone-beta boswellic acid (AKBA), In sinefungin, S-adenosylmethionine, S- adenosyl-homocysteine, Delisea furanone and N- sulfonyl homoserine Ester.

101. a kind of method for the gastrointestinal disorder for treating subject with this need, this method includes applying medicine to subject Learn the pharmaceutical composition of any one of embodiment 1 to 100 of active dose.

102. the method for embodiment 101, wherein the gastrointestinal disorder is inflammatory bowel disease (IBD) or irritable bowel syndrome (IBS)。

103. the method for embodiment 101, wherein the gastrointestinal disorder is selected from ulcerative colitis, Crohn disease, not really Qualitative colitis, mucous colitis, collagenous colitis, chronic bacillary diarrhea (johne's disease), microscopic colitis, idiopathic are scorching Property enteropathy and the relevant colitis of antibiotic, ischemic colitis, metastatic colitis, pseudomembranous colitis and lymphatic Colitis.

104. the method for embodiment 101, wherein the gastrointestinal disorder is ulcerative colitis.

105. the method for embodiment 104, wherein ulcerative colitis is selected from proctitis ulcerosa, proctosigmoid Scorching, left sided colitis and general ulcerative colitis.

106. the method for embodiment 104, wherein the method is by the ulcerative colitis disease activity index of patient (UCDAI) at least 10%, 20%, 30%, 50%, 60%, 70%, 80% or 90% are reduced after treatment 8 weeks.

107. the method for embodiment 104, wherein the administration carries out daily.

108. the method for embodiment 104, wherein the application continues at least 1,2,3,4,5,6,7,8,9 or 10 week.

109. the method for embodiment 104, wherein at least application is primary daily for the dosage, continue at least 2,3,4,5,6, 7,8,9,10,11,12,13,14 or 15 days.

110. the method for embodiment 104, wherein at least application is primary daily for the dosage, continue at least 1,2,3,4,5, 6,7,8,9,10,11 or 12 weeks.

111. the method for embodiment 104, wherein at least application is primary daily for the dosage, be continued up to 3,4,5,6,7, 8,9,10,11,12,13,14,15,16,17,18,19 or 20 days.

112. the method for embodiment 104, wherein at least application is primary daily for the dosage, be continued up to 1,2,3,4,5, 6,7,8,9,10,11 or 12 weeks.

113. the method for embodiment 104 continues two days at least continuous wherein the dosage is at least applied twice daily.

114. the method for embodiment 104, wherein the dosage is at least applied twice daily, continue at least 3,4,5,6,7, 8,9,10,11,12,13,14 or 15 days.

115. the method for embodiment 104, wherein the dosage is at least applied twice daily, continue at least 1,2,3,4,5, 6,7,8,9,10,11 or 12 weeks.

116. the method for embodiment 104, wherein the dosage is at least applied twice daily, be continued up to 3,4,5,6,7, 8,9,10,11,12,13,14,15,16,17,18,19 or 20 days.

117. the method for embodiment 104, wherein the dosage is applied at least twice daily, be continued up to 1,2,3,4,5, 6,7,8,9,10,11 or 12 weeks.

118. the method for embodiment 104 continues at least one day wherein the dosage is applied at least three times daily.

119. the method for embodiment 104, wherein the dosage is applied at least three times daily, continue at least 2,3,4,5,6, 7,8,9,10,11,12,13,14 or 15 days.

120. the method for embodiment 104, wherein the dosage is applied at least three times daily, be continued up to 2,3,4,5,6, 7,8,9,10,11,12,13,14 or 15 days.

121. the method according to any one of foregoing embodiments, wherein the method includes the first dosage regimen, Followed by second dosage regimen.

122. the method for embodiment 121, wherein the second dosage regimen includes the agent less than or equal to the first dosage regimen The maintenance dose of amount.

123. the method for embodiment 121, wherein the second dosage regimen continues at least about 2,4,6,8,10,12,18,24, 36,48,72 or 96 months.

124. the method for embodiment 121, wherein the second dosage regimen continues to continue.

125. the method for embodiment 121, wherein be divided at least about 1 between the first and second dosage regimens, 2,3, 4,5,6,7,8,9,10,11 or 12 weeks.

126. the method for embodiment 121, wherein the second dosage regimen is continuous dosing regimens.

127. the method for embodiment 121, wherein the second dosage regimen is intermittent dosing regimen.

128. the method for embodiment 121, wherein intermittent dosing regimen at least 1,2,3,4,5,6,7,8,9,10,11, 12,13 or 14 days treatment phases, followed by least 1,2,3,4,5,6,7,8,9,10,11,12,13 or 14 day quiescent stage.

129. the method for any one of foregoing embodiments, by nose duodenum, is led to wherein the application includes taking orally It crosses bowel lavage or passes through rectal suppository.

130. the method for any one of foregoing embodiments, wherein gastrointestinal tract ecological disturbance is eliminated or reduced to the method.

131. the method for any one of foregoing embodiments, the bacterium that wherein the method increases in subject's gastrointestinal tract is more Sample.

132. the method for any one of foregoing embodiments, wherein tested with antibiotic pretreatment before applying composition Person.

133. the method for embodiment 132, wherein the antibiotic is selected from Amoxicillin, tetracycline, metronidazole, Li Fubu Spit of fland, clarithromycin, Clofazimine, vancomycin, rifampin, nitroimidazole, chloramphenicol and combinations thereof；Optionally, antibiotic packet Include the antibiotic combinations scheme with Amoxicillin, tetracycline and metronidazole (ATM).

134. the method for embodiment 132, wherein the antibiotic is selected from rifaximin, Ryfamycin derivative, Li Fu Flat, Rifabutin, Rifapentine, rifalazil, amphomycin, aminoglycoside, gentamicin, neomycin, streptomysin, Ba Long are mould Element, verdamicin, mutamicin, sisomicin, Netilmicin, retymicin, kanamycins, aztreonam, aztreonam Macrolide, clarithromycin, Dirithromycin, roxithromycin, Ketek, azithromycin, bismuth subsalicylate, vancomycin, chain Mycin, feldamycin, amikacin, Arbekacin, neomycin, Netilmicin, paromomycin, erythromycin, tobramycin, An Pu Mycin and combinations thereof.

135. the method for any one of foregoing embodiments, wherein tested with anti-inflammatory agent pretreatment before applying composition Person.

136. the method for any one of foregoing embodiments, wherein this method eliminate or reduce it is one or more, 2 kinds or more It is a variety of, 3 kinds or more, 4 kinds or more symptom, the symptoms are selected from diarrhea, spasm, tenesmus, weight loss, go out Blood, loss of appetite, abdominal pain, fever, fatigue, anaemia, inflammation and microulceration.

137. the method for any one of foregoing embodiments, wherein this method further includes application 5-aminosalicylic acid agent, skin Matter steroids, immunosuppressor or combinations thereof.

138. the method for any one of foregoing embodiments, wherein this method further comprising administering to 5-aminosalicylic acid or its spread out Biology, sulfasalazine or derivatives thereof or combinations thereof.

139. the method for any one of foregoing embodiments, wherein applying biofilm disruption before applying pharmaceutical composition Agent.

140. the method for any one of foregoing embodiments, wherein applying biofilm disruption after applying pharmaceutical composition Agent.

The method of any one of 141. foregoing embodiments, wherein biofilm disruption agent is administered simultaneously with pharmaceutical composition.

142. methods according to any one of previous embodiment, wherein the method also includes removing the attached of subject Record.

The method of the illness or illness of 143. treatment subject with this need, the method includes applying to the subject The pharmaceutical composition of any one of embodiment 1 to 100 with pharmacy active dose effectively treats the illness or illness, Wherein disorder or illness are selected from acne, AIDS enteropathy, the relevant gastroenteritis of AIDS, whole body alopecia, senile dementia, starch Sample denaturation, amyotrophic lateral sclerosis, ankylosing spondylitis, apositia, antibiotic-associated colitis, Asbergers are comprehensive Sign, attention deficit disorder (ADD), attention deficit hyperactivity disorder (ADHD), autism spectrum disorder (ASD), Behcet are comprehensive Simulator sickness, chronic clostridium difficile infection (CDI), chronic constipation, chronic depression, chronic fatigue syndrome (CFS), chronic idiopathic False obstructive syndrome, chronic inflammation Demyelinating Polyneuropathy, chronic nausea, chronic urticaria, celiaca, glue Former colitis, polyp of colon, constipation mainly have FBD, Crohn disease, cryptogenic cirrhosis, cyclicity vomiting, dermatitis herpetiformis, Diabetes, familial Mediterranean fever, fatty liver, functional bowel disorder (FBD), gastroesophageal reflux, Gillian-Barre syndrome, Glomerulonephritis, hemolytic uremic syndrome, halitosis, based on IBS constipation, based on IBS diarrhea/constipation alternating, IBS diarrhea, IBS based on pain, it is Idiopathic Thrombocytopenic Purpura (ITP), idiopathic/simple constipation, uncertain colitis, inflammatory Enteropathy (IBD), irritable bowel syndrome (IBS), adolescent diabetes, Lyme disease, manic-depressive psychosis, metabolic syndrome, micro- knot Enteritis, migraine, Combination cryoglobulinemia, mucous colitis, multiple sclerosis, myasthenia gravis, NASH (non-wine Essence steatohepatitis), non-rheumatoid arthritis, non-rheumatoid factor positive arthritis, non-ulcer dyspepsia, Nuo Wo Gram viral gastroenteritis, obesity, obsessive-compulsive disorder, pain, FBD, Parkinson's disease, panarteritis, polyposis, primary biliary Cirrhosis, primary clostridial infection (CDI), primary sclerotic cholangitis (PSC), pseudomembranous colitis, spirit Characteristic of disease disease, Reiter syndrome, recurrent diverticulitis, Rett syndrome, rheumatoid arthritis, brandy nose, rotavirus Gastroenteritis, sacro-iliitis, schizophrenia, chorionitis, dry syndrome, small bowel overgrowth, sudden infant death syndrome (SIDS), systemic loupus erythematosus, ulcerative colitis, upper abdomen FBD, vascular inflammatory disease, viral gastroenteritis, diabetes Pre syndrome, type-1 diabetes mellitus, type-2 diabetes mellitus, depression, schizophrenia and emotional handicap.

A kind of 144. methods for the IBD for treating subject with this need, this method include applying pharmacy to subject to live First antibiotic of property dosage or probiotics are to inhibit or antagonism Fusobacterium strain.

The method of 145. embodiments 144, wherein Fusobacterium species be selected from F.nucleatum, actinomyces pseudonecrophorus and F.varium。

The method of 146. embodiments 144 or 145, wherein the first probiotics includes pula clostridium species.

The method of 147. embodiments 144 or 145, wherein the first probiotics includes pula clostridium.

The method of 148. embodiments 144, wherein the method further applies pharmaceutical active dosage to the subject The second antibiotic or probiotics to inhibit or antagonism Mycobacterium species.

The method of 149. embodiments 148, wherein the Mycobacterium species are perituberculosis mycobacterium (MAP).

The method of 150. embodiments 148 or 149, wherein probiotics include selected from by corynebacteria, Dietzia, Gordonia, mycobacteria, Nocard's bacillus, beam village Salmonella, Skermania, butyric acid tomb village bacterium, Turicella, Rhodococcus sp and One of anti-myco group of Williamsia composition or it is a variety of, two or more, 3 kinds or more, 4 kinds or more, 5 Kind or more, 6 kinds or more or 7 kinds or more.

The method of a kind of 151. treatments or the IBD for treating subject with this need, this method comprises: removal subject Appendix is applied biofilm disruption agent to subject, to subject's administration of antibiotics, and is given in subject's embodiment 1 to 100 The pharmaceutical active dosage of the pharmaceutical composition of any one.

A kind of 152. methods, the growth stimulant including applying pula clostridium species to subject, and collected from subject Fecal specimens are to prepare fecal microorganism composition.

The method of 153. embodiments 152, wherein the fecal microorganism composition includes relative to from identical tested The raised levels of pula clostridium species of the control fecal microorganism composition (not taking the growth stimulant) of person.

The method of 154. embodiments 152 or 153, wherein subject's orally ingestible growth stimulant.

155. method as described in any one of embodiment 152 to 154, wherein the growth stimulant is selected from Apples Glue, N-acetyl-glucosamine, cysteine, glutathione, riboflavin and flavine.

156. method as described in any one of embodiment 152 to 155, wherein the fecal specimens are in application growth thorn It is collected at least about 1,2,3,4,5,6,7,8,9,10,11,12,13,14,18,20,24,28,30 or 36 hour after swashing agent.

The method of any one of 157. embodiments 152 to 155, wherein at least about 1 after applying growth stimulant, 2,3, 4,5 or 6 days collection fecal specimens.

The method of any one of 158. embodiments 152 to 155, wherein before collecting fecal specimens, by growth stimulation Agent was applied to subject more than about 1,2,3,4,5,6,7,8,9,10,11,12,13 or 14 day.

The method of any one of 159. embodiments 152 to 155, wherein applying stimulant before collecting fecal specimens It is more than 1,2,3,4,5,6,7,8,9,10,11,12,13 or 14 week for subject.

160. method as described in any one of embodiment 152 to 155, wherein the growth stimulant daily at least 1, 2, it is applied to the subject 3,4,5,6,7,8,9 or 10 times.

The method of any one of 161. embodiments 152 to 155, wherein the fecal microorganism composition is identical as coming from The control fecal microorganism composition (not applying growth stimulant) of subject is compared, comprising 1.5 times or more, 2 times or more More times, 2.5 times or more, 3 times or more, 3.5 times or more, 4 times or more, 5 times or more, 10 times or More times, 50 times or more, 100 times or more, the pula clostridium of 1000 times or more or 10,000 times or more Bacterium.

The method of any one of 162. embodiments 152 to 155, wherein fecal microorganism composition is relative to from identical The control fecal microorganism composition (not applying growth stimulant) of subject includes at least 10% or more, 15% or more, 20% Above, 25% or more, 30% or more, 40% or more, 50% or more, 60% or more, 70% or more, 80% or more, 90% with It is upper, 100% or more, 150% or more, 200% or more, 250% or more, 300% or more, 350% or more, 400% or more, 450% or more, 500% or more, 600% or more, 700% or more or 800% or more pula clostridium bacterium.

The method of any one of 163. embodiments 152 to 155 further comprises generating medicine group from fecal microorganism Close object.

The method of 164. embodiments 163, wherein pharmaceutical composition includes about 10³To about 10¹³, about 10⁴To about 10¹², about 10⁵To about 10¹¹, about 10⁶To about 10¹⁰, about 10⁷To about 10⁹Or about 10⁷To about 10⁸Between the pula clostridium bacterium that survives.

The method of 165. embodiments 163, wherein the preparation of pharmaceutical composition is without at alcohol treatment, detergent Reason, heat treatment, radiation and the processing being ultrasonically treated.

The method of 166. embodiments 163, wherein the preparation of pharmaceutical composition includes at alcohol treatment, detergent Reason, the processing step of heat treatment, radiation and ultrasonic treatment.

The method of 167. embodiments 163, wherein the preparation of pharmaceutical composition includes being selected from density gradient, filtering and chromatography The separating step of method.

The method of 168. embodiments 163, wherein the preparation of pharmaceutical composition does not include selected from density gradient, filtering and color The separating step of spectrometry.

Embodiment

Embodiment 1. treats ulcerative colitis

If meeting following one or more standards, select the patient of HBI >=7 by giving fecal microorganism composition Treated: the age is more than 18 years old male and female patient；Ulcerative colitis is determined by pervious colonoscopy (UC) diagnosis has consistent histology and clinical process；UC refers at least to proctosigmoid region；Start in research When by colonoscopy confirm activity；Slightly to moderate recurrent UC, it is defined as ulcerative colitis disease activity index (UCDAI) scoring is from 3 to 8；Research starts the preceding symptom (recurrent events) less than 4 weeks；Minimum scope when UCDAI screening is commented It is divided into 3 points (mucous membrane appearances)；At least 4 weeks before the study began with consistent dose (at least 1.6 grams/day of mesalazine or Balsalazide At least 4.5 grams/day) it uses oral 5-aminosalicylic acid (5-ASA) and/or enters preceding at least three moon in research with consistent dose Use imuran (at least 1.5mg/kg/ days) or Ismipur (at least 1mg/kg/ days).

Following standard is for excluding certain patients: the presence of Crohn disease or useless fellow dermatitis；UCDAI scoring is greater than 8 points (need emergency operation or there are serious diseases)；Oral steroid is used in 4 weeks before the study began；Before entering research most Antibiotic is used in 2 weeks afterwards；The variation of 5-ASA dosage is taken orally before research starts and during research in entire 8 weeks in last 4 weeks or is ground Study carefully the variation that Ismipur and imuran drug dose are taken orally in first 3 months；Before entering research or entire 8 weeks study Rectum 5-ASA or steroids are used in 1 week of period；Prescription medicine or over the counter probiotics system are used in 2 weeks before the study began Agent；NSAID (non-steroidal anti-inflammatory drugs) is used 1 week before 8 weeks research phases and during entire research.

All conventional ulcerative colitis are cut out within patient at least one week before giving fecal microorganism composition to control It treats.In addition, before giving blend composition, patient's anti-inflammatory agent (such as Mesalazine) and/or one or more anti-is given Raw element.Blend composition can also (such as aluminium hydroxide, magnesium hydroxide, dimethicone be antiacid containing acid inhibitor, antiacid Agent), H2 antagonist (such as ranitidine), proton pump inhibitor (such as Omeprazole) or combinations thereof.Drug described herein Composition once a day oral administration.Every patient receives constant dosage；However, the volume of dosage may depend on weight.

The abdominal symptoms and intestines of 3 days upon administration, 1 week, 1 month, 3 months, 6 months, 9 months and 12 months assessment patients Outer performance

Due to that can be carried out without departing from the scope of the disclosure to construction described and illustrated herein and method Various modifications, thus include front description in all the elements should be interpreted it is illustrative rather than restrictive. The range and range of the disclosure should not be limited by any of above exemplary embodiment, and should according only to appended claims and its Equivalent limits.All patents and non-patent literature quoted in this specification are incorporated herein by reference in their entirety.

A kind of pancolitis treatment method of the fecal microorganism rich in pula clostridium bacterium of embodiment 2.

One 8 years old female patient, with 2 years pancolitis medical histories, with the fecal microorganism for being rich in pula clostridium bacterium Treatment.Based on steroids, the prior treatment of immunosuppressor and anti-inflammatory agent is largely not suitable for the patient.Patient is daily 7-8 bloody stool is continued through, with mucus, it will be apparent that the sense of urgency and abdominal pain, until giving fecal microorganism transplanting (FMT).

For FMT, she is treated in advance with rifaximin, metronidazole and vancomycin, and is retained in imuran (Imuran) and on budesonide.After some improvement for realizing gut function, the fresh donor excrement that she experienced 5 days is derivative Full spectrum micropopulation FMT.Followed by since in late December, 2013 daily and mother together as contributor family Bowel lavage.Patient has reached the excrement of forming, can return to school, and experienced growth spurt.Steroids is reduced, Imuran It is such.However, daily bowel lavage usually requires prevention recurrence.Such case continues, and more than 650 families donate bowel lavage, Most of every 7 days 6-7 times, stool is still soft, slight urgent and visible mucus mostly.

In order to further improve the state of an illness of patient, pula clostridium bacterium growth stimulation is given to excrement donor (mother) and patient Object.Before and after mother takes orally feeding apple pectin (and later n-acetyl-glucosamine) daily, test donor [mother] F.prausnitzii bacterial content in excrement.After donor supplements apple pectin and n-acetyl-glucosamine, donor excrement Endogenous F.prausnitzii bacterial content rises about 10⁴.After supplement in 7 days, the stool quality change dramatically of receptor daughter becomes Must be harder, become less frequently, without mucus, urgency disappears, and bowel lavage frequency is down to 4-5 bowel lavage/week.Change this After kind, the oral supplement of the identical apple pectin of daughter or n-acetyl-glucosamine is given, excrement is caused to be formed and stopped Some further improvement of the ability of budesonide.Daughter continues to use family bowel lavage FMT, but her excrement is formed more, and And it usually requires with lower frequency bowel lavage (every 7 days bowel lavage 4 times).

Embodiment 3: pula clostridium bacterium-enrichment diet, the treatment for the colitis disease based on fecal microorganism group

One 24 years old female patient suffers from serious colitis during international travel.Her bloody diarrhea is very serious, Her hemoglobin drops to 3.0 or so, this level is typically considered fatal.She receives repeatedly to transfuse blood and resistive connection enteritis Treatment.

Part is restored, she returns to Australia, she is sent to hospital there, and finds her serious pancolitis still Very trippingly bleeding.Anti-inflammatory agent, including steroids, 6-MP, 5-ASA compound and intravenous fluid are applied, and carries out iron Infusion.She seeks second of view to therapeutic scheme, because while there is maximum therapeutic scheme, and plans to carry out colon Resection, but her hemoglobin remains at 9-10 or so.

In repeating colonoscopy, find she with lasting patch shape colitis, only some healing areas, but big The blood that majority oozes out when being Sigmoidoscope and mucosal contact.Culture is negative to C.difficile bacterium and other pathogens , and she continues to ooze out blood from mucous membrane, while in entire colon visible vessels loss, but terminal ileum is unaffected.

She starts to receive the treatment based on fecal microorganism group, to prevent colectomy.Her symptom is obviously improved, blood Lactoferrin rises between 10 to 11.However, she can not be restored to hemoglobin water before 13-14 years old or so Normal Colon inflammation It is flat.

Interview her mother, i.e. excrement donor, it is proposed that contain apple pectin, N-acetyl-glucosamine and inulin by giving her Special diet increase the content of her intestinal microbiota pula clostridium.Mother and daughter go home to continue family's excrement bowel lavage Treatment takes pula clostridium bacterium-enhancing diet with contributor.

Behind fecal microorganism group treatment 12 weeks rich in pula clostridium bacterium, the hemoglobin of patient rises to 13.2 for the first time To between 14.5, and the quantity of excrement enema treatment can be reduced to twice a week by her mother from daily.

After three months, patient has carried out follow-up colonoscopy.In colonoscopy, her mucous membrane is largely cured Merging shows visible tiny mucous membrane blood vessel.Lumen excrement shows serious colon from the perspective of Sigmoidoscope in " ball " Scorching healing.Still there is blood once in a while to mix with excrement, shows still there is mucous membrane spot to need to heal.Not by any scientific theory beam It ties up, the significant variation of patient blood hemoglobin shows the excrement composition for changing donor of contributor's diet, this changes in turn The microorganism group of receptor is become to help to cure the lining in colonic cavity.Again, not by the constraint of any scientific theory, this The ability of kind reduction bleeding due to caused by metatrophia and exudation makes patient from colectomy-, and this is mainly due to pulas The growth of clostridium.

Claims

1. a kind of pharmaceutical composition, comprising the fecal microorganism from single donor subject, the subject apply it is a kind of or A variety of pula clostridium species or one or more growth stimulants at least one pula clostridium species, wherein the excrement Microorganism includes relative to the control excrement from the identical donor subject for not applying one or more growth stimulants The elevated levels of at least one pula clostridium species of microorganism.

2. pharmaceutical composition described in claim 1, wherein the donor subject absorbs one or more pula clostridiums Strain or one or more growth stimulants.

3. pharmaceutical composition described in claim 1, wherein one or more growth stimulants are selected from by apple pectin, N- The group of acetylglucosamine, cysteine, glutathione, riboflavin and flavine composition.

4. pharmaceutical composition described in claim 1, wherein the elevated levels are selected from 1.5 times or more, 2 times or more Again, 2.5 times or more, 3 times or more, 3.5 times or more, 4 times or more, 5 times or more, 10 times or more, 50 times or more, 100 times or more, 1000 times or more and 10,000 times or more.

5. pharmaceutical composition, comprising being able to suppress or more than first non-pathogenic microorganisms living of Fusobacterium species and can press down More than second non-pathogenic microorganisms living of system or antagonism Mycobacterium species.

6. pharmaceutical composition described in claim 5, wherein the Fusobacterium species are selected from actinomyces pseudonecrophorus, tool core shuttle bar Bacterium, F.canifelinum, F.gonidiaformans, fusobacterium mortiferum, F.naviforme, fusobacterium necrogenes, F.russii, Ulcer Fusobacterium and F.varium.

7. pharmaceutical composition described in claim 5, wherein the Mycobacterium species are perituberculosis mycobacterium (MAP).

8. pharmaceutical composition as claimed in claim 7, wherein more than described first non-pathogenic microorganism living includes pula clostridium Strain.

9. pharmaceutical composition described in claim 5, wherein more than described second non-pathogenic microorganism living includes selected from by stick Shape bacillus, Dietzia, Gordonia, mycobacteria, Nocard's bacillus, beam village Salmonella, Skermania, butyric acid tomb village bacterium, Turicella, Rhodococcus sp and Williamsia composition one of anti-myco group or it is a variety of, two or more, 3 kinds or more A variety of, 4 kinds or more, 5 kinds or more, 6 kinds or more or 7 kinds or more.

10. pharmaceutical composition described in claim 1, wherein described pharmaceutical composition also includes fecal microorganism preparation.

11. pharmaceutical composition described in any one of claim 10, wherein the fecal microorganism preparation includes the complete or basic of donor Complete microorganism.

12. pharmaceutical composition described in any one of claim 10, wherein the fecal microorganism preparation includes the micro- life of non-selected excrement Object.

13. pharmaceutical composition described in any one of claim 10, wherein the fecal microorganism preparation lack selected from amino acid coccus, Ah Gram graceful bacterium, Alistipes, Anaerotruncus, Bacteroides, Bifidobacterium, Blaw spy Salmonella, Butyrivibrio, shuttle Bacterium, Collins Salmonella, fecal bacteria, corynebacteria, Dorea, enterococcus, Escherichia, Eubacterium, haemophilus, Holdemania, lactic acid bacteria, catarrhalis, Parabacteroides, Prey irrigate bacterium, Propionibacterium, Raoul bacterium, caecum sieve This Salmonella, Ruminococcus, staphylococcus, streptococcus, rare micrococcus and at least one, at least two kinds of of Veillonella, at least 3 Kind or at least four kinds of bacteriums.

14. a kind of method for treating IBD in subject with this need, the method includes applying pharmacy to the subject First antibiotic of active dose or probiotics are to inhibit or antagonism shuttle Caulobacter species.

15. method of claim 14, wherein the Fusobacterium species are selected from F.nucleatum, actinomyces pseudonecrophorus and F.varium。

16. method of claim 14, wherein first probiotics includes pula clostridium species.

17. method of claim 14, wherein first probiotics includes pula clostridium.

18. method of claim 14, wherein the method further applies pharmaceutical active dosage to the subject Second antibiotic or probiotics are to inhibit or antagonism Mycobacterium species.

19. method of claim 18, wherein the Mycobacterium species are perituberculosis mycobacterium (MAP).

20. method of claim 18, wherein the probiotics include selected from by corynebacteria, Dietzia, Gordonia, mycobacteria, Nocard's bacillus, beam village Salmonella, Skermania, butyric acid tomb village bacterium, Turicella, Rhodococcus sp and One of anti-myco group of Williamsia composition or it is a variety of, two or more, 3 kinds or more, 4 kinds or more, 5 Kind or more, 6 kinds or more or 7 kinds or more.